CN113962585A - Carbon source performance evaluation method and system - Google Patents

Carbon source performance evaluation method and system Download PDF

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CN113962585A
CN113962585A CN202111270712.1A CN202111270712A CN113962585A CN 113962585 A CN113962585 A CN 113962585A CN 202111270712 A CN202111270712 A CN 202111270712A CN 113962585 A CN113962585 A CN 113962585A
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carbon source
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蒋富海
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Csd Water Service Co ltd
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Abstract

The application provides a carbon source performance evaluation method, improvement and system, and relates to the field of carbon source performance evaluation and biological activity improvement, wherein the carbon source performance evaluation method comprises the following steps: obtaining a carbon source to be evaluated; performing various types of tests on the carbon source to be evaluated to obtain a plurality of test results; judging whether the multiple test results meet the respective corresponding evaluation standards; and outputting the qualified evaluation result when the plurality of test results meet the respective corresponding evaluation standards. By implementing the implementation mode, the performance of the carbon source can be automatically (man-machine interactive) evaluated, so that the quality control of the carbon source is realized, and the improvement of the efficiency of the carbon source use and the standardization of the quality control are facilitated.

Description

Carbon source performance evaluation method and system
Technical Field
The application relates to the field of carbon source performance evaluation and biological activity improvement, in particular to a carbon source performance evaluation method and system.
Background
At present, the quality control of various carbon sources is not perfect, and many manufacturers directly feed the carbon sources on a machine when the carbon sources are not subjected to qualitative, semi-quantitative or quantitative evaluation tests so as to hopefully improve the production efficiency. However, in practice, it has been found that when the availability of carbon sources is poor, the denitrification performance for biochemical reactions is unstable, the total nitrogen removal efficiency is not high, or excessive addition cannot be utilized or absorbed by microorganisms, such carbon sources are likely to cause toxicity by microorganisms or increase pollution indexes such as COD. Therefore, the quality control of the carbon source is imperative.
Disclosure of Invention
The embodiment of the application aims to provide a method and a system for evaluating carbon source performance, which can automatically evaluate the carbon source performance, so that the quality control of a carbon source is realized, and the improvement of the carbon source use efficiency and the quality control standardization are facilitated.
In a first aspect, an embodiment of the present application provides a method for evaluating performance of a carbon source, where the method includes:
obtaining a carbon source to be evaluated;
performing various types of tests on the carbon source to be evaluated to obtain a plurality of test results;
judging whether the plurality of test results meet respective corresponding evaluation standards;
and outputting the qualified evaluation result when the plurality of test results meet the respective corresponding evaluation standards.
In the implementation process, the method can be used for carrying out various automatic (man-machine interactive) tests on the carbon source to be evaluated, and automatically evaluating a plurality of obtained automatic evaluation results so as to output evaluation qualified results when the evaluation of the carbon source to be evaluated is qualified. Therefore, the implementation of the embodiment can automatically evaluate the performance of the carbon source, so that the quality control of the carbon source is realized, and the improvement of the efficiency of the carbon source use and the standardization of the quality control are facilitated.
Further, after the outputting of the qualified evaluation result, the method further comprises:
and feeding the carbon source to be evaluated on a machine.
Further, the step of obtaining the carbon source to be evaluated comprises:
obtaining a carbon source to be treated;
identifying the carbon source to be treated to obtain a carbon source class;
and when the carbon source is a long-chain carbon source, activating and improving the carbon source to be treated to obtain the carbon source to be evaluated.
Further, the step of performing a plurality of types of tests on the carbon source to be evaluated to obtain a plurality of test results comprises:
performing physical and chemical index detection on the carbon source to be evaluated to obtain a first test result;
performing biotoxicity detection on the carbon source to be evaluated to obtain a second test result;
carrying out denitrification load detection on the carbon source to be evaluated to obtain a third test result;
and carrying out COD (chemical oxygen demand) biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result.
Further, the step of performing biotoxicity detection on the carbon source to be evaluated to obtain a second test result comprises:
and carrying out clear water aeration on the carbon source to be evaluated to detect the biotoxicity, and obtaining a second test result.
Further, the step of performing denitrification load detection on the carbon source to be evaluated to obtain a third test result comprises:
and carrying out anoxic stirring on the carbon source to be evaluated to detect denitrification load, and obtaining a third test result.
Further, the step of performing COD biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result includes:
and carrying out aerobic aeration on the carbon source to be evaluated to detect the biochemical degradation limit of COD so as to obtain a fourth test result.
A second aspect of the embodiments of the present application provides a carbon source performance evaluation system, including:
the acquisition unit is used for acquiring the carbon source to be evaluated;
the testing unit is used for carrying out multi-type testing on the carbon evaluation source to be tested to obtain a plurality of testing results;
the judging unit is used for judging whether the plurality of test results meet the corresponding evaluation standards;
and the output unit is used for outputting the qualified evaluation result when the plurality of test results meet the corresponding evaluation standards.
In the implementation process, the device system performs multiple types of automatic (man-machine interactive) tests on the carbon source to be evaluated, and performs automatic evaluation on multiple obtained automatic evaluation results, so that the evaluation qualified result is output when the evaluation of the carbon source to be evaluated is qualified. Therefore, the implementation of the embodiment can automatically evaluate the performance of the carbon source, so that the quality control of the carbon source is realized, and the improvement of the efficiency of the carbon source use and the standardization of the quality control are facilitated.
A third aspect of the embodiments of the present application provides an electronic device, including a memory and a processor, where the memory is used to store a computer program, and the processor runs the computer program to make the electronic device execute the method for evaluating performance of a carbon source according to any one of the first aspect of the embodiments of the present application.
A fourth aspect of the embodiments of the present application provides a computer-readable storage medium, which stores computer program instructions, and when the computer program instructions are read and executed by a processor, the method for evaluating carbon source performance according to any one of the first aspect of the embodiments of the present application is performed.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present application, the drawings that are required to be used in the embodiments of the present application will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present application and therefore should not be considered as limiting the scope, and that those skilled in the art can also obtain other related drawings based on the drawings without inventive efforts.
FIG. 1 is a schematic flow chart of a method for evaluating carbon source performance provided in the examples of the present application;
FIG. 2 is a schematic flow chart of another method for evaluating carbon source performance provided in the examples of the present application;
FIG. 3 is a schematic system diagram of a carbon source performance evaluation system provided in an embodiment of the present application;
fig. 4 is a schematic structural diagram of a carbon source performance evaluation system provided in an embodiment of the present application.
Detailed Description
The technical solutions in the embodiments of the present application will be described below with reference to the drawings in the embodiments of the present application.
It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures. Meanwhile, in the description of the present application, the terms "first", "second", and the like are used only for distinguishing the description, and are not to be construed as indicating or implying relative importance.
Example 1
Referring to fig. 1, fig. 1 is a schematic flow chart of a method for evaluating carbon source performance according to an embodiment of the present disclosure. The carbon source performance evaluation method comprises the following steps:
s101, obtaining a carbon source to be evaluated.
S102, performing multi-type tests on the carbon source to be evaluated to obtain a plurality of test results.
S103, judging whether the multiple test results meet the respective corresponding evaluation standards, if so, executing a step S104; if not, the flow is ended.
And S104, outputting the evaluation qualified result.
In this embodiment, the method can be used for performance evaluation of coupling modification of a Carbon Source (CS) and Activated Sludge (AS) for heterotrophic denitrification, and is also beneficial to improving denitrification utilization efficiency.
And S105, feeding the carbon source to be evaluated on a computer.
In the embodiment of the present application, the execution subject of the method may be a computing system such as a computer and a server, and the embodiment is not limited in any way.
In this embodiment, an execution subject of the method may also be an intelligent device such as a smart phone and a tablet computer, which is not limited in this embodiment.
It can be seen that, by implementing the carbon source performance evaluation method described in this embodiment, multiple types of automated (human-computer interactive) tests can be performed on the carbon source to be evaluated, and the obtained multiple automated (human-computer interactive) evaluation results can be automatically evaluated, so that the evaluation qualified result is output when the evaluation of the carbon source to be evaluated is qualified. Therefore, the implementation of the embodiment can automatically (man-machine interactive) evaluate the performance of the carbon source, so that the quality control of the carbon source is realized, and the improvement of the efficiency of the carbon source use and the standardization of the quality control are facilitated.
Example 2
Please refer to fig. 2, fig. 2 is a schematic flow chart of a method for evaluating carbon source performance according to an embodiment of the present application. As shown in fig. 2, the method for evaluating the performance of a carbon source comprises the following steps:
s201, obtaining a carbon source to be treated.
S202, identifying the carbon source to be processed to obtain the carbon source variety.
In this example, the carbon source types were classified into two types:
firstly, if the carbon source is acetic acid, acetates (sodium acetate), monohydric alcohols (such as methanol) and dihydric alcohols (such as ethanol), the carbon source is short-chain and easy to utilize;
② long-chain carbon source if the carbon source is polyhydric alcohol (such as propanol and glycerol), saccharide (such as glucose and sucrose), starch (flour and corn steep liquor), and composite carbon source (prepared by mixing more than one single product).
And S203, when the carbon source is a long-chain carbon source, activating the carbon source to be processed to obtain the carbon source to be evaluated.
In this example, the activation modification of peat was performed on a long-chain carbon source. If the carbon source is the above-mentioned second type long-chain carbon source, it needs to be activated because it is a macromolecular organic carbon source and its utilization rate as a direct carbon source is low. If the carbon source is the short-chain easily-utilized carbon source of the first class, the carbon source can be directly and quickly utilized and absorbed due to the fact that the carbon source is organic acid or organic alcohol which is easy to degrade and utilize by small molecules, and the carbon source can directly enter a simulation evaluation link of different concentrations and dosages of the carbon source without activation so as to evaluate the performance of the carbon source.
S204, performing physical and chemical index detection on the carbon source to be evaluated to obtain a first test result.
In this example, the method first adds a carbon source (volume about 200-500mL), then measures the pH of the carbon source, and manually assays COD, BOD, TN (to evaluate the B/C ratio, C/N ratio, B/N ratio, i.e., carbon source equivalent and its biodegradability). Wherein, the method quantitatively judges whether the conformity indexes are as follows: the COD equivalent is not less than 20 ten thousand, the BOD/COD ratio is more than 0.7, the COD/TN ratio is not less than 500: 1, the pH value is within the range of 2.0-8.0. If so, the evaluation criteria are considered to be met, and the subsequent steps are executed.
S205, performing biotoxicity detection on the carbon source to be evaluated to obtain a second test result.
In this embodiment, the method may be to introduce the clear water in advance, and then add the carbon source (gradually increasing the gradient of the mass concentration at 100-. On the basis, whether the compliance indexes are as follows is judged quantitatively: whether the vital signs (life habits) of the fish indicator organism b1 are normal or not is observed for 0.5-2 h (if the vital signs are normal, the condition that if the carbon source is added to a certain concentration range in the range of 1, no harm is caused to microorganisms can be indirectly judged). If so, the evaluation criteria are considered to be met, and the subsequent steps are executed.
As an alternative embodiment, the step of performing a biotoxicity test on the carbon source to be evaluated to obtain the second test result comprises:
and (4) carrying out clear water aeration on the carbon source to be evaluated to detect the biotoxicity, and obtaining a second test result.
S206, carrying out denitrification load detection on the carbon source to be evaluated to obtain a third test result.
In this embodiment, the method may first add about 1000-3000mL of active sludge source, and synchronously add carbon source (with a mass concentration of 80-500mg/L), and then stir it. And (3) manually sampling and detecting the initial and final TN concentration change of the reaction by reacting for 2-5 h. On the basis, whether the compliance indexes are as follows is judged quantitatively: whether the removal concentration of TN reaches the expectation and whether the ton water of the removal unit TN is lower than the expectation is used as a qualitative (or semi-quantitative) index for evaluating the denitrification efficiency. If so, the evaluation criteria are considered to be met, and the subsequent steps are executed.
As an alternative embodiment, the step of performing denitrification load detection on the carbon source to be evaluated to obtain a third test result comprises:
and carrying out anoxic stirring on the carbon source to be evaluated to detect the denitrification load, and obtaining a third test result.
And S207, carrying out COD biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result.
In this embodiment, the method may first add about 1000-3000mL of active sludge source, then add carbon source (with a mass concentration of 80-500mg/L), and then aerate it. After the reaction is carried out for 10-18 h, the change of the filtered COD (i.e. sCOD) concentration at the initial and final reaction stages is detected by manual sampling. On the basis, whether the compliance indexes are as follows is judged quantitatively: the removal rate of sCOD is more than 85 percent, and the concentration of residual COD (sCOD) after the final filtration of the reaction is less than 50mg/L, which is used as a qualitative (or semi-quantitative) index of the biochemical degradation limit of COD.
As an alternative embodiment, the step of performing COD biochemical degradation limit detection on the carbon source to be evaluated to obtain the fourth test result comprises:
and carrying out aerobic aeration on the carbon source to be evaluated to detect the biochemical degradation limit of COD so as to obtain a fourth test result.
S208, judging whether the first test result, the second test result, the third test result and the fourth test result meet respective corresponding evaluation criteria, if so, executing steps S209-S210; if not, the flow is ended.
And S209, outputting the evaluation qualified result.
S210, feeding the carbon source to be evaluated on a machine.
In this embodiment, the method may be used to normally add the carbon source on the machine after the evaluation that the performance of the native (or modified) carbon source is qualified. If the carbon source is not qualified, the carbon source needs to be replaced and reselected for identification modification and new evaluation, and the on-machine administration can be carried out after the evaluation is qualified.
It can be seen that, by implementing the carbon source performance evaluation method described in this embodiment, multiple types of automated (human-computer interactive) tests can be performed on the carbon source to be evaluated, and the obtained multiple automated (human-computer interactive) evaluation results can be automatically evaluated, so that the evaluation qualified result is output when the evaluation of the carbon source to be evaluated is qualified. Therefore, the implementation of the embodiment can automatically (man-machine interactive) evaluate the performance of the carbon source, so that the quality control of the carbon source is realized, and the improvement of the efficiency of the carbon source use and the standardization of the quality control are facilitated.
Example 3
Please refer to fig. 3, fig. 3 is a schematic structural diagram of a carbon source performance evaluation system according to an embodiment of the present application. As shown in fig. 3, the carbon source performance evaluation system includes:
an obtaining unit 310, configured to obtain an evaluation carbon source to be detected;
the testing unit 320 is used for performing various types of tests on the carbon source to be evaluated to obtain a plurality of test results;
a determining unit 330, configured to determine whether the multiple test results meet respective corresponding evaluation criteria;
and the output unit 340 is used for outputting the qualified evaluation result when the plurality of test results meet the corresponding evaluation standards.
As an alternative embodiment, the carbon source performance evaluation system further comprises:
and the production unit 350 is used for feeding the carbon source to be evaluated on a computer.
In this embodiment, the production unit 350 may obtain an additional carbon source similar to the carbon source to be evaluated, and machine-feed the carbon source.
As an optional implementation, the obtaining unit 310 includes:
an obtaining subunit 311, configured to obtain a carbon source to be processed;
an identifier unit 312, configured to identify a carbon source to be processed to obtain a carbon source type;
and the activator unit 313 is used for activating the carbon source to be processed to obtain the carbon source to be evaluated when the carbon source is a long-chain carbon source.
As an alternative embodiment, the test unit 320 includes:
the first detecting subunit 321 is configured to perform physical and chemical index detection on the carbon source to be evaluated to obtain a first test result;
the second detection subunit 322 is configured to perform biological toxicity detection on the carbon source to be evaluated to obtain a second test result;
the third detection subunit 323 is configured to perform denitrification load detection on the carbon source to be evaluated to obtain a third test result;
and the fourth detection subunit 324 is configured to perform COD biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result.
As an alternative embodiment, the second detecting subunit 322 is specifically configured to perform clear water aeration on the carbon source to be evaluated to detect biological toxicity, so as to obtain a second test result.
As an alternative embodiment, the third detecting subunit 323 is specifically configured to perform anaerobic stirring on the carbon source to be evaluated to detect the denitrification load, so as to obtain a third test result.
As an alternative embodiment, the fourth detecting subunit 324 is specifically configured to perform aerobic aeration on the carbon source to be evaluated to detect the biochemical degradation limit of COD, so as to obtain a fourth test result.
In this embodiment, in fig. 4, the carbon source performance evaluation system may specifically include a biochemical sludge source system 1, an activated sludge efficiency improving system 2, a carbon source storage and supply system 3, a carbon source efficiency evaluation system 4, an evaluation sludge supply system 5, and an enzymatic activated nutrient 6. Wherein, the obtaining unit 310 comprises a biochemical sludge source system 1, an activated sludge efficiency improving system 2, a carbon source storage and supply system 3 and an enzymatic activated nutrient 6; the test unit 320 includes a carbon source efficiency evaluation system 4 and an evaluation sludge supply system 5.
Referring to fig. 4, fig. 4 is a schematic structural diagram of a carbon source performance evaluation system. It is mainly noted that the subsequent numbers will be described with reference to fig. 4, and redundant description is not repeated in this embodiment.
In this embodiment, the biochemical sludge source system 1 can be an anoxic tank or an aerobic aeration tank containing a biochemical active mixed liquid as an active sludge source.
In the embodiment, the activated sludge efficiency improving system 2 comprises an activated sludge transfer tank 21 (5-15 m)3Effective volume with stirring device), transfer-in pump 221 (5-10 m)3The flow range of/h, the pump is used for pumping sludge from the biochemical sludge source system 1), and the pump 222 is used for transferring the sludge (5-10 m)3The flow range of the flow is/h, the activated sludge transfer tank 21 is used for taking sludge and pumping the sludge to the carbon source storage tank 31), and pipelines (connecting pipelines of the activated sludge transfer tank 21 and the biochemical sludge source system 1 and the activated sludge transfer tank 21 and the carbon source storage tank 31).
In the present embodiment, the carbon source storage and supply system 3 includes a carbon source storage tank 31 (20)~40m3Effective volume, stirring device and magnetic turning plate liquid level meter, metering dosing pump 32 (flow range of 50-500L/h), and dosing pipeline accessory 33. The medicine pipeline accessory 33 is divided into two pipelines 331 and 332 (respectively provided with a valve c1/c2), wherein the pipeline 331 is connected into the biochemical sludge source system 1, the pipeline 332 is connected into the carbon source efficiency evaluation system 4, and the pipelines 332 are respectively provided with a 1-a 4 sub-gates which are respectively connected into the 41-44 subsystems. Into which a carbon source to be evaluated or modified is filled.
In this embodiment, the carbon source efficiency evaluation system 4 includes a physicochemical index detection subsystem 41, a biological toxicity judgment subsystem 42, a denitrification load verification subsystem 43, and a COD biochemical degradation limit verification subsystem 44. The effective volume of 41-44 is 1-5L (column or cylinder structure). A physicochemical detection device b1 (containing a handheld pH pen) is arranged in the physicochemical index detection subsystem 41; clear water and clear water fish (such as small individual goldfish, crucian carp and the like) indicating organisms b2 are arranged in the biological toxicity judgment subsystem 42, and an oxygen increasing micro-power device b3 is arranged; a stirring power device b4 is arranged in the denitrification load verification subsystem 43; the COD biochemical degradation limit verification subsystem 44 is internally provided with a micro aeration power device b 5.
In this embodiment, the first detecting subunit 321 corresponds to the physicochemical index detecting subsystem 41, the second detecting subunit 322 corresponds to the biotoxicity determining subsystem 42, the third detecting subunit 323 corresponds to the denitrification load verifying subsystem 43, and the fourth detecting subunit 324 corresponds to the COD biochemical degradation limit verifying subsystem 44.
In this embodiment, the detection process in the physicochemical index detection subsystem 41 is as follows: starting the pump 32, the valve C2 (closing the valve C1) and the stop valve a1, adding a carbon source (the volume is about 200-: the COD equivalent is not less than 20 ten thousand, the BOD/COD ratio is more than 0.7, the COD/TN ratio is not less than 500: 1, the pH value is within the range of 2.0-8.0. If the above-mentioned match, enter the next procedure.
In this embodiment, the detection process in the biological toxicity judgment subsystem 42 is as follows: introducing clear water into the biological toxicity judgment subsystem 42 in advance, starting the pump 32, the valve c2 (the valve is closed, the valve is c1) and the stop valve a2, adding a carbon source into the biological toxicity judgment subsystem 42 (gradually increasing the gradient of the mass concentration at 100-: whether the vital signs (life habits) of the fish indicator organism b1 are normal or not is observed for 0.5-2 h (if the vital signs are normal, the condition that if the carbon source is added to a certain concentration range in the range of 1, no harm is caused to microorganisms can be indirectly judged). If the above-mentioned match, enter the next procedure.
In this embodiment, the detection process in the denitrification load verification subsystem 43 is as follows: starting a pump 51 and a valve 53a (closing a valve 53b), and adding an active sludge source with the volume of about 1000-3000mL into the denitrification load verification subsystem 43 from the biochemical sludge source system 1; synchronously starting the pump 32, the valve c2 (closing the valve c1) and the valve a3, adding a carbon source (with the mass concentration of 80-500mg/L) into the denitrification load verification subsystem 43, and starting the stirring power device b4 for stirring. After reacting for 2-5 h, manually sampling and detecting the initial and final TN concentration change of the reaction, and quantitatively judging whether the conformity indexes are as follows: whether the removal concentration of TN reaches the expectation and whether the ton water of the removal unit TN is lower than the expectation is used as a qualitative (or semi-quantitative) index for evaluating the denitrification efficiency. If the above-mentioned match, enter the next procedure.
In this embodiment, the detection process in the COD biochemical degradation limit verification subsystem 44 is: starting a pump 51 and a valve 53b (closing a valve 53a), and adding an active sludge source with the volume of about 1000-3000mL into the COD biochemical degradation limit verification subsystem 44 from the biochemical sludge source system 1; synchronously starting the pump 32, the valve c2 (closing the valve c1) and the valve a4, adding a carbon source (with the mass concentration of 80-500mg/L) into the COD biochemical degradation limit verification subsystem 44, and starting the micro aeration power device b5 for aeration. After the reaction is carried out for 10-18 h, the change of the filtered COD (namely sCOD) concentration at the initial and final reaction stages is detected by manual sampling, and whether the compliance index is as follows is judged quantitatively: the removal rate of sCOD is more than 85 percent, and the concentration of residual COD (sCOD) after the final filtration of the reaction is less than 50mg/L, which is used as a qualitative (or semi-quantitative) index of the biochemical degradation limit of COD.
In this embodiment, the evaluation sludge supply system 5 includes a sludge supply micropump 51 (with a flow rate of 1-5L/h, which is connected to the sludge extraction from the biochemical sludge source system 1 and pumps the sludge to the denitrification load verification subsystem 43 or the COD biochemical degradation limit verification subsystem 44), and a pipeline 52 (a connecting pipeline between the biochemical sludge source system 1 and the COD biochemical degradation limit verification subsystem 44).
In the embodiment, the enzymatic activation nutrient 6 adopts hydrolytic enzymatic yeast as an activation modification auxiliary of a primary carbon source, and the addition amount of the hydrolytic enzymatic yeast to the carbon source storage tank 31 is 0.3-2 g/L mass concentration.
In this embodiment, when the carbon source is the above-mentioned second type long-chain carbon source, since all of the carbon sources are macromolecular organic carbon sources and the utilization rate of the carbon sources as direct carbon sources is low, activation is required, and the activation operation is as follows: the activated sludge efficiency-improving system 2 needs to be started, activated sludge is supplemented into the carbon source storage tank 31 for endogenous activation, the amount of the added sludge is such that the MLSS concentration in the activated sludge 31 is 500-1000 mg/L (MLVSS is 200-600 mg/L; the nitrate nitrogen concentration in the activated sludge static sedimentation liquid is less than 10mg/L), and the enzymatic activation nutrient 6 is synchronously supplemented into the carbon source storage tank 31. The activation time of the mud/carbon source/yeast three-phase mixed material is generally 8-24 h. If the carbon source is a short-chain easily-utilized carbon source of the first class: since the carbon source is organic acid or organic alcohol which is easy to degrade and utilize by small molecules and can be directly and quickly utilized and absorbed, the carbon source can directly enter a simulation evaluation link of carbon sources with different concentrations and dosages without activation so as to evaluate the performance of the carbon source.
In this embodiment, after the performance of the native (or modified) carbon source is determined to be in accordance with the performance, the pump 32 and the valve c1 (the valve c2 is closed) are turned on, and the carbon source is normally added into the biochemical sludge source system 1. If not, the carbon source is replaced and reselected for identification modification and new evaluation, and the on-machine administration can be carried out after the evaluation is qualified.
In the embodiment of the present application, for the explanation of the carbon source performance evaluation system, reference may be made to the description in embodiment 1 or embodiment 2, and details are not repeated in this embodiment.
It can be seen that, by implementing the carbon source performance evaluation system described in this embodiment, the system can perform automated (human-computer interactive) evaluation on the performance of the carbon source, so as to implement quality control on the carbon source, and further facilitate improvement of the efficiency of carbon source usage and standardization of quality control.
The embodiment of the application provides an electronic device, which comprises a memory and a processor, wherein the memory is used for storing a computer program, and the processor runs the computer program to enable the electronic device to execute the carbon source performance evaluation method in any one of embodiment 1 or embodiment 2 of the application.
The embodiment of the present application provides a computer-readable storage medium, which stores computer program instructions, and when the computer program instructions are read and executed by a processor, the method for evaluating the performance of a carbon source according to any one of embodiment 1 or embodiment 2 of the present application is performed.
In the several embodiments provided in the present application, it should be understood that the disclosed system and method may be implemented in other ways. The above-described system embodiments are merely illustrative, and for example, the flowchart and block diagrams in the figures illustrate the architecture, functionality, and operation of possible implementations of systems, methods and computer program products according to various embodiments of the present application. In this regard, each block in the flowchart or block diagrams may represent a module, segment, or portion of code, which comprises one or more executable instructions for implementing the specified logical function(s). It should also be noted that, in some alternative implementations, the functions noted in the block may occur out of the order noted in the figures. For example, two blocks shown in succession may, in fact, be executed substantially concurrently, or the blocks may sometimes be executed in the reverse order, depending upon the functionality involved. It will also be noted that each block of the block diagrams and/or flowchart illustration, and combinations of blocks in the block diagrams and/or flowchart illustration, can be implemented by special purpose hardware-based systems which perform the specified functions or acts, or combinations of special purpose hardware and computer instructions.
In addition, functional modules in the embodiments of the present application may be integrated together to form an independent part, or each module may exist separately, or two or more modules may be integrated to form an independent part.
The functions, if implemented in the form of software functional modules and sold or used as a stand-alone product, may be stored in a computer readable storage medium. Based on such understanding, the technical solution of the present application or portions thereof that substantially contribute to the prior art may be embodied in the form of a software product stored in a storage medium and including instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the steps of the method according to the embodiments of the present application. And the aforementioned storage medium includes: a U-disk, a removable hard disk, a Read-Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk or an optical disk, and other various media capable of storing program codes.
The above description is only an example of the present application and is not intended to limit the scope of the present application, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, improvement and the like made within the spirit and principle of the present application shall be included in the protection scope of the present application. It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures.
The above description is only for the specific embodiments of the present application, but the scope of the present application is not limited thereto, and any person skilled in the art can easily conceive of the changes or substitutions within the technical scope of the present application, and shall be covered by the scope of the present application. Therefore, the protection scope of the present application shall be subject to the protection scope of the claims.
It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other identical elements in a process, method, article, or apparatus that comprises the element.

Claims (10)

1. A method for assessing the performance of a carbon source, the method comprising:
obtaining a carbon source to be evaluated;
performing various types of tests on the carbon source to be evaluated to obtain a plurality of test results;
judging whether the plurality of test results meet respective corresponding evaluation standards;
and outputting the qualified evaluation result when the plurality of test results meet the respective corresponding evaluation standards.
2. The method for evaluating the performance of a carbon source according to claim 1, wherein after outputting the evaluation qualification result, the method further comprises:
and feeding the carbon source to be evaluated on a machine.
3. The method for evaluating the carbon source performance according to claim 1, wherein the step of obtaining the carbon source to be evaluated comprises:
obtaining a carbon source to be treated;
identifying the carbon source to be treated to obtain a carbon source class;
and when the carbon source is a long-chain carbon source, activating the carbon source to be treated to obtain the carbon source to be evaluated.
4. The method for evaluating the carbon source performance as claimed in claim 1, wherein the step of performing a plurality of types of tests on the carbon source to be evaluated to obtain a plurality of test results comprises:
performing physical and chemical index detection on the carbon source to be evaluated to obtain a first test result;
performing biotoxicity detection on the carbon source to be evaluated to obtain a second test result;
carrying out denitrification load detection on the carbon source to be evaluated to obtain a third test result;
and carrying out COD (chemical oxygen demand) biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result.
5. The method for evaluating the carbon source performance according to claim 4, wherein the step of performing biotoxicity test on the carbon source to be evaluated to obtain a second test result comprises the following steps:
and carrying out clear water aeration on the carbon source to be evaluated to detect the biotoxicity, and obtaining a second test result.
6. The method for evaluating the carbon source performance as claimed in claim 4, wherein the step of performing denitrification load detection on the carbon source to be evaluated to obtain a third test result comprises:
and carrying out anoxic stirring on the carbon source to be evaluated to detect denitrification load, and obtaining a third test result.
7. The method for evaluating the carbon source performance according to claim 4, wherein the step of performing COD biochemical degradation limit detection on the carbon source to be evaluated to obtain a fourth test result comprises the following steps:
and carrying out aerobic aeration on the carbon source to be evaluated to detect the biochemical degradation limit of COD so as to obtain a fourth test result.
8. A carbon source performance evaluation system, comprising:
the acquisition unit is used for acquiring the carbon source to be evaluated;
the testing unit is used for carrying out multi-type testing on the carbon evaluation source to be tested to obtain a plurality of testing results;
the judging unit is used for judging whether the plurality of test results meet the corresponding evaluation standards;
and the output unit is used for outputting the qualified evaluation result when the plurality of test results meet the corresponding evaluation standards.
9. An electronic device, comprising a memory for storing a computer program and a processor for executing the computer program to cause the electronic device to perform the carbon source performance assessment method according to any one of claims 1 to 7.
10. A readable storage medium, wherein computer program instructions are stored, which when read and executed by a processor, perform the method for carbon source performance assessment according to any one of claims 1 to 7.
CN202111270712.1A 2021-10-29 2021-10-29 Carbon source performance evaluation method and system Pending CN113962585A (en)

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