Clean room grade processing method and device

Through the clean control platform, the purification level of the operating room is dynamically adjusted, which solves the energy waste problem caused by traditional fixed-level design and achieves more efficient energy utilization.

CN119826302APending Publication Date: 2025-04-15张华
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Patent Information

Application Number
CN202510159314.4
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-02-13
Publication Date
2025-04-15

AI Technical Summary

Technical Problem

In traditional clean operating room design, fixed purification levels lead to energy waste, making it difficult to dynamically adjust air cleanliness according to different surgical needs.

Method used

Provide a method and device for dynamically adjusting the clean room level. Through the clean control platform, it obtains real-time data, calculates the difference value and adjusts the air purification equipment to achieve dynamic adjustment of the operating room purification level.

Benefits of technology

It effectively solves the energy waste problem caused by fixed purification levels, and can dynamically adjust the purification level of the operating room according to actual needs to improve energy utilization efficiency.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention discloses a clean room grade processing method and device, and relates to the technical field of medical clean operating rooms. In the method, a purification request sent by a target person is responded, the purification request is a request for adjusting the purification level of a target clean room, and the target clean room is any operating room; determining a first purification level according to the purification request; acquiring first data corresponding to the target clean room; determining that the target clean room is currently at a second purification level according to the first data; determining a first value based on the first data, and determining a second value according to the first purification level; calculating a difference value between the first numerical value and the second numerical value; and the target equipment is adjusted according to the difference value, so that the target clean room is controlled to be adjusted from the second purification level to the first purification level. By implementing the technical scheme provided by the invention, the problem of unnecessary energy waste caused by the fact that a current operating room is designed to be at a fixed purification level is effectively solved.
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Description

Technical Field

[0001] The present application relates to the technical field of medical clean operating rooms, and in particular to a method and device for processing the clean room level. Background Art

[0002] In the medical field, especially in the operating room environment, the requirements for air cleanliness are extremely strict, which is mainly due to the high attention paid to patient safety, surgical success rate and overall medical quality. The application of clean operating rooms is not only an important symbol of medical technology progress, but also provides a solid foundation for the successful implementation of various complex and high-risk operations. However, the difference in the type of surgery and its risk level directly determines the cleanliness level required in the operating room.

[0003] Traditionally, clean operating rooms are often designed as spaces with fixed purification levels. This design model lacks flexibility in dealing with air cleanliness, and it is difficult to respond promptly to the dynamic changes in air cleanliness requirements at different stages of operation or when facing different surgical needs. Specifically, the fixed-level design model may lead to unnecessary waste of energy because the operating room still needs to maintain a fixed level of purification at a higher energy consumption when the highest clean level requirements are not met.

[0004] Therefore, there is an urgent need for a clean room level processing method and device that can solve the above technical problems. Summary of the invention

[0005] The present application provides a method and device for processing the clean room level, which can dynamically adjust the purification level of the operating room according to actual needs, effectively solving the problem of unnecessary energy waste caused by the current operating room being designed with a fixed purification level.

[0006] In a first aspect, the present application provides a method for processing the clean room level, which is applied to a clean control platform, and the method includes: responding to a purification request sent by a target personnel, the purification request is a request for adjusting the purification level of a target clean room, and the target clean room is any operating room; determining a first purification level according to the purification request; obtaining first data corresponding to the target clean room; determining that the target clean room is currently at a second purification level according to the first data; determining a first value based on the first data, and determining a second value according to the first purification level; calculating the difference between the first value and the second value; adjusting the target device according to the difference, so as to control the target clean room to be adjusted from the second purification level to the first purification level, and the target device is a device installed in the target clean room for air purification.

[0007] By adopting the above technical solution, it is possible to respond to the purification request sent by the target personnel, determine the required first purification level according to the purification request, obtain the first data corresponding to the target clean room, and understand the current air quality status of the operating room in real time. The difference between the first value determined based on the first data and the second value determined according to the first purification level is calculated, so that the adjustment of the air purification equipment is more accurate. The target equipment is adjusted according to the difference, which can ensure that the operating room smoothly transitions from the current second purification level to the required first purification level. The purification level of the operating room can be dynamically adjusted according to actual needs, which effectively solves the problem of unnecessary energy waste caused by the current operating room being designed with a fixed purification level.

[0008] Optionally, determining that the target clean room is currently in the second purification level based on the first data specifically includes: obtaining a first particle concentration value in the target clean room; comparing the first particle concentration value with a preset standard threshold to obtain a third purification level; obtaining a third value, the third value including an air supply volume value, a pressure difference value, a temperature and humidity value, and a target gas concentration value; comparing the third value with a preset value corresponding to the third purification level; if the third value is consistent with the preset value, confirming that the target clean room is currently in the third purification level, and outputting the third purification level as the second purification level.

[0009] By adopting the above technical solution, the first particle concentration value in the target clean room is obtained, and the first particle concentration value is compared with the preset standard threshold value, so that the current purification level of the clean room (i.e., the third purification level) can be accurately determined. The third value is also obtained, and the third value is compared with the preset value corresponding to the third purification level, so as to verify whether the clean room has actually reached the required purification level. When the third value is consistent with the preset value, it is confirmed that the target clean room is currently in the third purification level and it is output as the second purification level. This process enables managers to quickly understand the current status of the clean room and make corresponding adjustments as needed.

[0010] Optionally, after adjusting the target device according to the difference so as to control the target clean room from the second purification level to the first purification level, the method also includes: obtaining a first air supply volume value and a pressure difference value corresponding to the target clean room at the first moment; judging whether the first air supply volume is within a preset air supply volume threshold, and whether the pressure difference value is within a preset pressure difference threshold, the first purification level including a preset air supply volume threshold and a preset pressure difference threshold; when the first air supply volume is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, confirming that the target device is in the first adjustment end state.

[0011] By adopting the above technical solution, the first air supply volume value and the pressure difference value corresponding to the target clean room at the first moment are obtained, so that the air flow and the pressure difference state in the clean room can be accurately monitored. When the first air supply volume is within the preset air supply volume threshold and the pressure difference value is within the preset pressure difference threshold, it is confirmed that the target device is in the first adjustment end state, and the adjustment process is detected in real time. When the preset state is reached, the adjustment operation can be stopped.

[0012] Optionally, when the first air supply volume is within a preset air supply volume threshold and the pressure difference value is within a preset pressure difference threshold, after confirming that the target clean room is in a first adjustment end state, the method also includes: obtaining a second particle concentration value and a temperature and humidity value corresponding to the target clean room at a second moment, the second moment being after the first moment; judging whether the second particle concentration value is within a preset particle concentration threshold and whether the temperature and humidity values ​​are within a preset temperature and humidity threshold, the first purification level includes a preset particle concentration threshold and a preset temperature and humidity threshold; when the second particle concentration value is within the preset particle concentration threshold and the temperature and humidity values ​​are within the preset temperature and humidity threshold, confirming that the target device is in a second adjustment end state; determining that the target clean room is in an adjustment completion state based on the first adjustment end state and the second adjustment end state, the adjustment completion state indicating that the target device has adjusted the target clean room from the second purification level to the first purification level.

[0013] By adopting the above technical solution, the second particle concentration value and temperature and humidity value corresponding to the target clean room at the second moment (after the first moment) are obtained, and the comprehensive monitoring of the clean room environmental quality is realized. It is ensured that the target device is confirmed to be in the second adjustment end state only when the second particle concentration value and the temperature and humidity value are both within the preset threshold. This dual judgment mechanism improves the efficiency and accuracy of the adjustment, and avoids the situation where the overall environment is mistakenly believed to have met the requirements because a single parameter has reached the standard. Combined with the first adjustment end state (based on the judgment of the air supply volume and pressure difference value) and the second adjustment end state (based on the judgment of the particle concentration and the temperature and humidity value), it can be more comprehensively confirmed whether the target clean room is in the adjustment completion state.

[0014] Optionally, after determining whether the second particle concentration value is within the preset particle concentration threshold and whether the temperature and humidity values ​​are within the preset temperature and humidity thresholds, the method also includes: when the second particle concentration value is not within the preset particle concentration threshold and the temperature and humidity values ​​are not within the preset temperature and humidity thresholds, confirming that the target device is in an adjustment unfinished state, and determining that the target clean room is in an adjustment state based on the adjustment unfinished state.

[0015] By adopting the above technical solution, when the second particle concentration value and the temperature and humidity values ​​do not meet the preset thresholds at the same time, it can be immediately confirmed that the target device is in an unfinished adjustment state, and based on this, it can be judged that the target clean room is still in an adjustment state, and it is clear that the target device is in an unfinished adjustment state, and it is necessary to continue to adjust the target device until all environmental parameters meet the preset thresholds.

[0016] Optionally, after confirming that the target clean room is in the first purification level, second data is obtained; it is determined whether the second data is consistent with preset data; when the second data is inconsistent with the preset data, it is confirmed that the target clean room is in an abnormal state, and early warning measures are determined according to the abnormal state.

[0017] By adopting the above technical solution, after confirming that the target clean room is in the first purification level, the second data is obtained and compared with the preset data, so that the environmental quality of the clean room can be accurately monitored. Once it is found that the second data is inconsistent with the preset data, it indicates that the target clean room may be in an abnormal state, and a quick response can be made and early warning measures can be taken, thereby effectively preventing potential environmental problems.

[0018] Optionally, the target device is adjusted according to the difference, specifically including: when the difference is the air volume value, the air supply device is adjusted according to the air volume value, and the air supply device is output as the target device; when the difference is the dust particle value, the number of air filter devices is adjusted according to the dust particle value, and the air filter device is output as the target device.

[0019] By adopting the above technical solution, for the difference in air volume values, the air supply equipment is adjusted according to the air volume value. This adjustment strategy can ensure that the air volume provided by the air supply equipment matches the actual needs of the clean room, thereby maintaining the air flow and pressure difference state in the clean room within the preset range. For the difference in dust particle values, the number of air filter devices is adjusted according to the dust particle values. It can ensure that the dust particle concentration in the air is effectively controlled to meet the purification level requirements of the clean room.

[0020] In a second aspect of the present application, a device for processing the level of a clean room is provided, the device is a clean control platform, the clean control platform includes a receiving unit, a processing unit and an adjustment unit; the receiving unit responds to a purification request sent by a target person, the purification request is a request for adjusting the purification level of a target clean room, the target clean room is any operating room; the first data corresponding to the target clean room is obtained; the processing unit determines a first purification level according to the purification request; determines that the target clean room is currently at a second purification level according to the first data; determines a first value based on the first data, and determines a second value according to the first purification level; calculates the difference between the first value and the second value; the adjustment unit adjusts the target device according to the difference, so as to control the target clean room to be adjusted from the second purification level to the first purification level, the target device is a device installed in the target clean room for air purification.

[0021] Optionally, the receiving unit is used to obtain a first particle concentration value in the target clean room; the processing unit is used to compare the first particle concentration value with a preset standard threshold to obtain a third purification level; the receiving unit is used to obtain a third value, the third value includes an air supply volume value, a pressure difference value, a temperature and humidity value, and a target gas concentration value; the processing unit is used to compare the third value with a preset value corresponding to the third purification level; if the third value is consistent with the preset value, it is confirmed that the target clean room is currently in the third purification level, and the third purification level is output as the second purification level.

[0022] Optionally, the receiving unit is used to obtain a first air supply volume value and a pressure difference value corresponding to the target clean room at a first moment; the processing unit is used to determine whether the first air supply volume is within a preset air supply volume threshold, and whether the pressure difference value is within a preset pressure difference threshold, and the first purification level includes a preset air supply volume threshold and a preset pressure difference threshold; when the first air supply volume is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, it is confirmed that the target device is in the first adjustment end state.

[0023] Optionally, the receiving unit is used to obtain a second particle concentration value and a temperature and humidity value corresponding to the target clean room at a second moment, and the second moment is after the first moment; the processing unit is used to determine whether the second particle concentration value is within a preset particle concentration threshold, and whether the temperature and humidity values ​​are within a preset temperature and humidity threshold, and the first purification level includes a preset particle concentration threshold and a preset temperature and humidity threshold; when the second particle concentration value is within the preset particle concentration threshold, and the temperature and humidity values ​​are within the preset temperature and humidity threshold, it is confirmed that the target device is in a second adjustment end state; the adjustment unit is used to determine that the target clean room is in an adjustment completion state according to the first adjustment end state and the second adjustment end state, and the adjustment completion state indicates that the target device has adjusted the target clean room from the second purification level to the first purification level.

[0024] Optionally, the adjustment unit is used to confirm that the target device is in an unfinished adjustment state when the second particle concentration value is not within the preset particle concentration threshold and the temperature and humidity values ​​are not within the preset temperature and humidity thresholds, and determine that the target clean room is in an adjustment state based on the unfinished adjustment state.

[0025] Optionally, the receiving unit is used to obtain second data after confirming that the target clean room is in the first purification level; the processing unit is used to determine whether the second data is consistent with the preset data; the adjustment unit is used to confirm that the target clean room is in an abnormal state when the second data is inconsistent with the preset data, and determine early warning measures according to the abnormal state.

[0026] Optionally, the processing unit is used to adjust the air supply equipment according to the air volume value when the difference is the air volume value, and output the air supply equipment as the target device; when the difference is the dust particle value, adjust the number of air filter devices according to the dust particle value, and output the air filter device as the target device.

[0027] In a third aspect of the present application, an electronic device is provided, which includes a processor, a memory, a user interface and a network interface, the memory is used to store instructions, the user interface and the network interface are used to communicate with other devices, and the processor is used to execute the instructions stored in the memory, so that an electronic device executes any one of the methods described above in the present application.

[0028] In a fourth aspect of the present application, a computer-readable storage medium is provided, wherein the computer-readable storage medium stores instructions, and when the instructions are executed, any one of the above methods of the present application is executed.

[0029] In summary, one or more technical solutions provided in the embodiments of the present application have at least the following technical effects or advantages: 1. It can respond to the purification request sent by the target personnel, determine the required first purification level according to the purification request, obtain the first data corresponding to the target clean room, and understand the current air quality status of the operating room in real time. The difference between the first value determined based on the first data and the second value determined according to the first purification level is calculated, so that the adjustment of the air purification equipment is more accurate. The target equipment is adjusted according to the difference, which can ensure that the operating room smoothly transitions from the current second purification level to the required first purification level. The purification level of the operating room can be dynamically adjusted according to actual needs, which effectively solves the problem of unnecessary energy waste caused by the current operating room being designed with a fixed purification level.

[0030] 2. Obtain the first particle concentration value in the target clean room, and compare the first particle concentration value with the preset standard threshold value, so as to accurately determine the current purification level of the clean room (i.e., the third purification level). Also obtain the third value, and compare the third value with the preset value corresponding to the third purification level to verify whether the clean room has actually reached the required purification level. When the third value is consistent with the preset value, it is confirmed that the target clean room is currently at the third purification level, and it is output as the second purification level. This process enables managers to quickly understand the current status of the clean room and make corresponding adjustments as needed. BRIEF DESCRIPTION OF THE DRAWINGS

[0031] Figure 1 It is a flow chart of a method for treating clean room level provided in an embodiment of the present application; Figure 2 It is a structural schematic diagram of a clean room level processing device provided in an embodiment of the present application; Figure 3 It is a structural schematic diagram of an electronic device disclosed in an embodiment of the present application.

[0032] Description of reference numerals: 201, receiving unit; 202, processing unit; 203, adjusting unit; 300, electronic device; 301, processor; 302, memory; 303, user interface; 304, network interface; 305, communication bus. DETAILED DESCRIPTION

[0033] In order to enable technicians in this field to better understand the technical solutions in this specification, the technical solutions in the embodiments of this specification will be clearly and completely described below in conjunction with the drawings in the embodiments of this specification. Obviously, the described embodiments are only part of the embodiments of this application, not all of the embodiments.

[0034] In the description of the embodiments of the present application, words such as "for example" or "for example" are used to indicate examples, illustrations or explanations. Any embodiment or design described as "for example" or "for example" in the embodiments of the present application should not be interpreted as being more preferred or more advantageous than other embodiments or designs. Specifically, the use of words such as "for example" or "for example" is intended to present related concepts in a specific way.

[0035] In the description of the embodiments of the present application, the meaning of the term "multiple" refers to two or more. For example, multiple systems refer to two or more systems, and multiple screen terminals refer to two or more screen terminals. In addition, the terms "first" and "second" are used for descriptive purposes only and cannot be understood as indicating or implying relative importance or implicitly indicating the indicated technical features. Thus, the features defined as "first" and "second" may explicitly or implicitly include one or more of the features. The terms "include", "comprise", "have" and their variations all mean "including but not limited to", unless otherwise specifically emphasized.

[0036] In the medical field, especially in the operating room environment, the requirements for air cleanliness are extremely strict, which is mainly due to the high attention paid to patient safety, surgical success rate and overall medical quality. The application of clean operating rooms is not only an important symbol of medical technology progress, but also provides a solid foundation for the successful implementation of various complex and high-risk operations. However, the difference in the type of surgery and its risk level directly determines the cleanliness level required in the operating room.

[0037] Traditionally, clean operating rooms are often designed as spaces with fixed purification levels. This design model lacks flexibility in dealing with air cleanliness, and it is difficult to respond promptly to the dynamic changes in air cleanliness requirements at different stages of operation or when facing different surgical needs. Specifically, the fixed-level design model may lead to unnecessary waste of energy because the operating room still needs to maintain a fixed level of purification at a higher energy consumption when the highest clean level requirements are not met.

[0038] Therefore, how to solve the problem of unnecessary energy waste caused by the current operating room being designed with a fixed purification level. A method for processing the clean room level provided in the embodiment of the present application is applied to a clean control platform. The clean control platform of the present application can be a platform that provides clean level control services for operating rooms. Figure 1 This is a flow chart of a method for treating a clean room level provided in an embodiment of the present application, with reference to Figure 1 The method includes the following steps S101-S107.

[0039] S101: responding to a purification request sent by a target person, where the purification request is a request for adjusting the purification level of a target clean room, and the target clean room is any operating room.

[0040] In the above S101, the target personnel refers to the operating room nurse, doctor or manager, and the target personnel sends a purification request through the touch screen interface, and the purification request includes the need to adjust the purification level of the target clean room, and the target clean room refers to any operating room. After receiving the purification request, the clean control platform parses the purification request to prepare for the next step.

[0041] S102: Determine a first purification level according to a purification request.

[0042] In the above S102, the clean control platform parses the purification request and determines the required first purification level. At this time, the first purification level is usually determined according to factors such as the type of surgery, the patient's health status, and the sterility requirements during the operation. This application predefines a purification level list, which includes three levels, namely, class 100 clean operating rooms, class 1,000 and class 10,000 clean operating rooms, and class 100,000 clean operating rooms. Among the three purification levels, class 100 clean operating rooms correspond to the highest level, followed by class 1,000 and class 10,000 clean operating rooms, and finally class 100,000 clean operating rooms. At this time, the first purification level is any purification level in the purification level list. Each purification level corresponds to a different air quality standard.

[0043] S103: Acquire first data corresponding to the target clean room.

[0044] In the above S103, the sensor is installed in the target clean room so as to obtain real-time data, i.e., first data, from the target clean room through the sensor network. The first data includes air volume data, pressure difference data, dust particle concentration data, temperature and humidity data, and urgent target air concentration data (such as specific bacteria or virus concentration). The first data reflects the current air quality status of the target clean room.

[0045] S104: Determine, according to the first data, that the target clean room is currently in the second purification level.

[0046] In the above S104, it is determined based on the first data that the target clean room is currently in the second purification level, specifically including: obtaining a first particle concentration value in the target clean room; comparing the first particle concentration value with a preset standard threshold to obtain a third purification level; obtaining a third value, the third value including an air supply volume value, a pressure difference value, a temperature and humidity value, and a target gas concentration value; comparing the third value with a preset value corresponding to the third purification level; if the third value is consistent with the preset value, confirming that the target clean room is currently in the third purification level, and outputting the third purification level as the second purification level.

[0047] Specifically, a particle concentration sensor is installed in the target clean room to monitor the particle concentration in the air in real time. The first particle concentration value is read regularly or in real time through a sensor network or a data interface. The read particle concentration data is preprocessed, such as denoising, smoothing, etc., to ensure the accuracy and reliability of the data. The first particle concentration value is compared with a preset standard threshold value. Since the predefined purification level list of this application contains three purification levels, and different purification levels correspond to different particle concentration thresholds, that is, one purification level corresponds to a particle concentration threshold. The threshold corresponding to each purification level is set according to the use requirements, industry standards or relevant regulations of the clean room. The first particle concentration value is compared with a plurality of preset standard thresholds to determine the purification level range to which it belongs. At this time, the preset standard thresholds include three types, and each threshold corresponds to a purification level. The first particle concentration value is compared with the three preset standard thresholds in turn, and the purification level corresponding to the value closest to and not greater than the first particle concentration value is selected as the third purification level. After determining that the first particle concentration value is at the third purification level, it is necessary to further verify other data in the target clean room to determine whether the target clean room is currently at the third purification level. The third value is compared with the preset value, which is the air supply value, the pressure difference value, the temperature and humidity value, and the target gas concentration value. The preset value is a preset range or standard value of the corresponding air supply value, pressure difference value, temperature and humidity value, and target gas concentration value obtained from the preset database according to the third purification level. Compare the parameters in the third value with the preset values ​​to determine whether they are consistent or meet the preset requirements. For the air supply value and the pressure difference value, it can be compared whether they are within the preset range. For the temperature and humidity values ​​and the target gas concentration value, it can be compared whether they are equal to or better than the preset standard value. If the third value is consistent with the preset value or meets the preset requirements, it is confirmed that the target clean room is currently in the third purification level. The third purification level is output as the second purification level (in this context, the second purification level is the current purification level after confirmation), which may be through a display screen or the like. By acquiring various data of the target clean room in real time, the current purification level of the target clean room can be accurately confirmed, and basic data support can be provided for subsequent environmental control and optimization.

[0048] Furthermore, when the first particle concentration value does not match the preset standard threshold, it is confirmed that the target clean room is not currently at the purification level, and the purification equipment needs to be controlled to re-purify the target clean room. When the third value is inconsistent with the preset value, it is confirmed that the target clean room is not currently at the third purification level, and the particle concentration value needs to be re-obtained, and the particle concentration value is re-compared with the preset standard threshold to determine a new purification level.

[0049] S105: Determine a first value based on the first data, and determine a second value according to the first purification level.

[0050] In the above S105, after obtaining the first data corresponding to the target clean room, multiple index values, namely the first numerical value, are calculated based on the first data, and the first numerical value is used to quantify the current air quality. Then, the second numerical value is determined based on the first purification level, and the second numerical value is a standard value or range preset based on the first purification level. These numerical values ​​involve multiple aspects such as dust particle concentration, temperature and humidity, and air flow rate.

[0051] S106: Calculate the difference between the first value and the second value.

[0052] In the above S106, after obtaining the first value corresponding to the current purification level of the target clean room, and then obtaining the second value corresponding to the first purification level to be adjusted, the difference or deviation between the first value and the second value is calculated to evaluate the gap between the current second purification level and the first purification level. In the clean room, necessary sensors and monitoring equipment are deployed, such as air volume sensors, dust particle counters, etc. These devices detect key parameters such as air volume and dust particle concentration in the clean room in real time or regularly. Collect and analyze these monitoring data to calculate the difference between the actual air volume value and the preset air volume value, or the difference between the actual dust particle value and the preset dust particle value. The preset air volume value and the preset dust particle value are usually set based on industry standards, historical data or actual needs. According to the calculation results, it is determined whether the difference is an air volume value or a dust particle value. In addition to the air volume and dust particles mentioned above, it is also necessary to monitor temperature and humidity, pressure difference, and harmful gas concentration.

[0053] S107: adjusting the target equipment according to the difference, so as to control the target clean room to be adjusted from the second purification level to the first purification level, the target equipment being equipment installed in the target clean room to perform air purification.

[0054] In the above S107, the target device is adjusted according to the difference, specifically including: when the difference is the air volume value, the air supply device is adjusted according to the air volume value, and the air supply device is output as the target device; when the difference is the dust particle value, the number of air filter devices is adjusted according to the dust particle value, and the air filter device is output as the target device. Specifically, when the difference is the air volume value, it is determined that the air supply device needs to be adjusted, that is, the target device is the air supply device. According to the difference size and direction (positive difference or negative difference) of the air volume value, a specific adjustment strategy is formulated. For example, if the actual air volume is less than the preset air volume, it may be necessary to increase the speed of the air supply device or open more air supply devices to increase the air volume. An adjustment instruction is sent to the air supply device through the control interface. The air supply device adjusts its working state according to the instruction, such as changing the speed, opening or closing, etc. When the difference is the dust particle value, the system determines that the air filter device needs to be adjusted. According to the difference size and direction of the dust particle value, the system formulates a specific adjustment strategy. For example, if the actual dust particle concentration is higher than the preset concentration, the system may need to increase the number of air filters, replace filters with higher efficiency, or strengthen filter maintenance. Send adjustment instructions to the air filter device through the control interface. The air filter device adjusts its working state according to the instructions, such as increasing the filter area, replacing the filter, etc. The air supply device and the air filter device can be accurately adjusted according to the air volume value or the dust particle value to ensure that the environmental parameters of the clean room meet the preset requirements.

[0055] In addition, adjustment measures are formulated based on the calculated difference. Adjustment measures may involve increasing or decreasing air volume, adjusting air velocity, adjusting temperature and humidity, etc. Instructions are sent to target devices (such as air purifiers, air conditioning systems, ventilation equipment, etc.) through control signals to implement adjustment strategies.

[0056] Further, in the process of adjusting the purification level of the target clean room, it is necessary to monitor the air quality data and make fine adjustments based on the feedback to ensure that the target clean room reaches the required first purification level, specifically including: obtaining the first air supply volume value and the pressure difference value corresponding to the first moment of the target clean room; judging whether the first air supply volume is within the preset air supply volume threshold, and whether the pressure difference value is within the preset pressure difference threshold, the first purification level includes the preset air supply volume threshold and the preset pressure difference threshold; when the first air supply volume is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, confirm that the target device is in the first adjustment end state. Specifically, in the target clean room, air supply volume sensors and pressure difference sensors are deployed respectively. These sensors can accurately and in real time monitor the air supply volume and pressure difference of the target clean room. After determining that the target device has been adjusted according to the difference, a time point is set as the first moment, and the first moment refers to any time point after the target device has been adjusted according to the difference. For example, the target device receives the adjustment instruction at 12:45:20, and can obtain the air supply volume value and pressure difference value of the target clean room at 12:47. At this time, 12:47 is the first moment. At the first moment, the data output by the air supply volume sensor and the pressure difference sensor are read through the sensor network or data interface. The read data is the first air supply volume value and the pressure difference value. According to the purification level requirements of the target clean room (the target clean room needs to be adjusted to the first purification level, and the first purification level already includes the preset air supply volume threshold and the preset pressure difference threshold). These thresholds are set according to the actual situation of the clean room, industry standards or relevant regulations. Compare the read first air supply volume value with the preset air supply volume threshold to determine whether it is within the threshold range. At the same time, compare the read pressure difference value with the preset pressure difference threshold to determine whether it is within the threshold range. If the first air supply volume value is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, it is determined that the current state of the target device meets the requirements of the first purification level. If the above conditions are met, it is confirmed that the target device is in the first adjustment end state. The first adjustment end state indicates that the target device has been adjusted to the air supply volume and pressure difference state that meet the requirements of the first purification level, and no further adjustment of the air supply volume and pressure difference is required. In addition, when the first air supply volume value is not within the preset air supply volume threshold, and the pressure difference value is not within the preset pressure difference threshold, it is confirmed that the target device is still in the adjustment state.

[0057] Further, after determining that the target device is in the first adjustment end state, it takes a period of time before other data of the target clean room can be monitored. Since other data need to be adjusted for a period of time before they can change, it is necessary to obtain other data of the target clean room at the second moment. Specifically, it includes: the second particle concentration value and temperature and humidity value corresponding to the second moment, and the second moment is after the first moment; judging whether the second particle concentration value is within the preset particle concentration threshold, and whether the temperature and humidity value is within the preset temperature and humidity threshold, and the first purification level includes the preset particle concentration threshold and the preset temperature and humidity threshold; when the second particle concentration value is within the preset particle concentration threshold, and the temperature and humidity value is within the preset temperature and humidity threshold, confirming that the target device is in the second adjustment end state; according to the first adjustment end state and the second adjustment end state, determining that the target clean room is in the adjustment completion state, the adjustment completion state indicates that the target device has adjusted the target clean room from the second purification level to the first purification level. Specifically, in the target clean room, particle concentration sensors, temperature sensors and humidity sensors are deployed. These sensors should be able to accurately and real-time monitor the particle concentration, temperature and humidity of the target clean room. A time point after the first moment is determined as the second moment, and this time point can be determined according to system settings, user requirements or actual detection requirements. At the second moment, the system reads the data output by the particle concentration sensor, the temperature sensor and the humidity sensor through the sensor network or the data interface. The read data is the second particle concentration value, the temperature value and the humidity value. According to the purification level requirements of the target clean room (i.e., the first purification level), the particle concentration threshold, the temperature threshold and the humidity threshold are preset in the system. The read second particle concentration value is compared with the preset particle concentration threshold to determine whether it is within the threshold range. At the same time, the read temperature value and humidity value are respectively compared with the preset temperature threshold and the humidity threshold to determine whether they are each within the threshold range. If the second particle concentration value is within the preset particle concentration threshold, and the temperature value and the humidity value are both within the preset temperature and humidity thresholds, it is determined that the current state of the target device meets the requirements of the first purification level. When the above conditions are met, it is confirmed that the target device is in the second adjustment end state. The second adjustment end state indicates that the target device has been adjusted to the particle concentration, temperature and humidity state that meet the requirements of the first purification level, and there is no need to further adjust the particle concentration, temperature and humidity of the target device. According to the air supply volume value and the pressure difference value at the first moment, it is judged whether the target device is in the first adjustment end state. Combined with the particle concentration value, temperature value and humidity value at the second moment, the judgment result is the second adjustment end state. If the target device is in the first adjustment end state and the second adjustment end state at the same time, it is confirmed that the target clean room is in the adjustment completion state. The adjustment completion state means that the target device has successfully adjusted the target clean room from the second purification level to the first purification level.It can accurately determine whether the target equipment is in the adjustment end state, and finally confirm whether the target clean room is in the adjustment completion state.

[0058] Furthermore, when the second particle concentration value is not within the preset particle concentration threshold, and the temperature and humidity value is not within the preset temperature and humidity threshold, it is confirmed that the target device is in an unfinished adjustment state, and the target clean room is determined to be in an adjustment state according to the unfinished adjustment state. Specifically, at the second moment, the second particle concentration value, temperature value and humidity value of the target clean room are read. These values ​​are compared with the preset particle concentration threshold, temperature threshold and humidity threshold. If the second particle concentration value is not within the preset particle concentration threshold range, that is, it is higher or lower than the upper or lower threshold limit. At the same time, the temperature value or the humidity value is also not within the preset temperature and humidity threshold range, that is, the temperature is higher or lower than the upper or lower threshold limit, or the humidity is higher or lower than the upper or lower threshold limit. According to the above comparison results, it is confirmed that the target device currently fails to meet the requirements of the first purification level. When one of these two conditions is not met, it is also confirmed that the target device currently fails to meet the requirements of the first purification level. It is determined that the target device is in an unfinished adjustment state, that is, the target device is still trying to adjust the various parameters of the target clean room to meet the preset threshold. Combined with the unfinished adjustment state of the target device and the current environmental parameters of the target clean room (second particle concentration value, temperature value and humidity value). Confirm that the target clean room is in the state of adjustment. This means that the target equipment is still being adjusted to improve the air quality and other environmental parameters of the target clean room until they meet the preset first purification level requirements. Only when both of the above conditions are met can it be confirmed that the target equipment meets the requirements of the first purification level.

[0059] In a possible implementation, it is possible to accurately determine whether the target clean room is in an abnormal state, and determine early warning measures according to the abnormal state, which helps to discover and solve problems in time and ensure that the target clean room is always kept within the required purification level, specifically including: after confirming that the target clean room is in the first purification level, obtaining the second data; judging whether the second data is consistent with the preset data; when the second data is inconsistent with the preset data, confirming that the target clean room is in an abnormal state, and determining early warning measures according to the abnormal state. Specifically, in the target clean room, necessary sensors and monitoring equipment, such as particle counters, temperature and humidity sensors, etc., are deployed. These devices monitor key parameters such as particle concentration, temperature and humidity in the clean room in real time or regularly. Collect and analyze these monitoring data to evaluate whether the target clean room meets the requirements of the first purification level. The first purification level generally includes a series of preset particle concentration thresholds, temperature thresholds, and humidity thresholds. If the monitoring data shows that all key parameters of the target clean room meet the requirements of the first purification level, the system confirms that the target clean room is in the first purification level. The second data refers to one or more groups of monitoring data further obtained by the system after confirming that the target clean room is in the first purification level. These data may include real-time monitoring values ​​or average values ​​over a period of time of key parameters such as particle concentration, temperature and humidity, and pressure difference. The second data is obtained in real time through the sensor network. The second data is compared with the preset data, which refers to a series of expected monitoring data values ​​or ranges that the system has set when confirming that the target clean room is in the first purification level. The second data is compared with the preset data to determine whether they are consistent. The comparison process may involve comparison of multiple parameters, such as comparison of particle concentration, comparison of temperature and humidity, etc. If the second data is consistent with the preset data within the allowable error range, it is considered that the state of the target clean room is stable. If there is a significant difference between the second data and the preset data, it is considered that the target clean room may be in an abnormal state. When the second data is inconsistent with the preset data, it is confirmed that the target clean room is in an abnormal state. The abnormal state may include excessive particle concentration, temperature and humidity deviating from the set range, abnormal pressure difference, etc. According to the specific type and severity of the abnormal state, the system determines the corresponding early warning measures. The early warning measures may include sending an alarm signal, starting a backup system, adjusting control parameters, etc. Further troubleshooting and repair processes can also be triggered to ensure that the target clean room can return to normal as soon as possible.

[0060] Through the above method, it is possible to respond to the purification request sent by the target personnel, determine the required first purification level according to the purification request, obtain the first data corresponding to the target clean room, and understand the current air quality status of the operating room in real time. The difference between the first value determined based on the first data and the second value determined according to the first purification level is calculated, so that the adjustment of the air purification equipment is more accurate. The target equipment is adjusted according to the difference, which can ensure that the operating room smoothly transitions from the current second purification level to the required first purification level. The purification level of the operating room can be dynamically adjusted according to actual needs, which effectively solves the problem of unnecessary energy waste caused by the current operating room being designed with a fixed purification level.

[0061] The present application also provides a clean room level processing device. Figure 2 This is a schematic diagram of a clean room level processing device provided in an embodiment of the present application, with reference to Figure 2 The device is a clean control platform, which includes a receiving unit 201, a processing unit 202 and an adjustment unit 203.

[0062] The receiving unit 201 responds to a purification request sent by a target person, where the purification request is a request for adjusting the purification level of a target clean room, where the target clean room is any operating room; and obtains first data corresponding to the target clean room.

[0063] The processing unit 202 determines a first purification level according to a purification request; determines that the target clean room is currently at a second purification level according to the first data; determines a first value based on the first data, and determines a second value according to the first purification level; and calculates a difference between the first value and the second value.

[0064] The adjustment unit 203 adjusts the target device according to the difference, so as to control the target clean room to be adjusted from the second purification level to the first purification level, wherein the target device is a device installed in the target clean room to perform air purification.

[0065] In one possible implementation, the receiving unit 201 is used to obtain a first particle concentration value in a target clean room; the processing unit 202 is used to compare the first particle concentration value with a preset standard threshold to obtain a third purification level; the receiving unit 201 is used to obtain a third value, the third value including an air supply volume value, a pressure difference value, a temperature and humidity value, and a target gas concentration value; the processing unit 202 is used to compare the third value with a preset value corresponding to the third purification level; if the third value is consistent with the preset value, it is confirmed that the target clean room is currently in the third purification level, and the third purification level is output as the second purification level.

[0066] In a possible implementation, the receiving unit 201 is used to obtain a first air supply volume value and a pressure difference value corresponding to the target clean room at a first moment; the processing unit 202 is used to determine whether the first air supply volume is within a preset air supply volume threshold, and whether the pressure difference value is within a preset pressure difference threshold, and the first purification level includes a preset air supply volume threshold and a preset pressure difference threshold; when the first air supply volume is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, it is confirmed that the target device is in the first adjustment end state.

[0067] In a possible implementation, the receiving unit 201 is used to obtain a second particle concentration value and a temperature and humidity value corresponding to a target clean room at a second moment, where the second moment is after the first moment; the processing unit 202 is used to determine whether the second particle concentration value is within a preset particle concentration threshold, and whether the temperature and humidity values ​​are within a preset temperature and humidity threshold, and the first purification level includes a preset particle concentration threshold and a preset temperature and humidity threshold; when the second particle concentration value is within the preset particle concentration threshold, and the temperature and humidity values ​​are within the preset temperature and humidity threshold, it is confirmed that the target device is in a second adjustment end state; the adjustment unit 203 is used to determine that the target clean room is in an adjustment completion state based on the first adjustment end state and the second adjustment end state, and the adjustment completion state indicates that the target device has adjusted the target clean room from the second purification level to the first purification level.

[0068] In one possible implementation, the adjustment unit 203 is used to confirm that the target device is in an unfinished adjustment state when the second particle concentration value is not within the preset particle concentration threshold and the temperature and humidity values ​​are not within the preset temperature and humidity thresholds, and determine that the target clean room is in an adjustment state based on the unfinished adjustment state.

[0069] In a possible implementation, the receiving unit 201 is used to obtain second data after confirming that the target clean room is in the first purification level; the processing unit 202 is used to determine whether the second data is consistent with the preset data; the adjustment unit 203 is used to confirm that the target clean room is in an abnormal state when the second data is inconsistent with the preset data, and determine early warning measures according to the abnormal state.

[0070] In one possible implementation, the processing unit 202 is used to adjust the air supply device according to the air volume value and output the air supply device as the target device when the difference is the air volume value; and to adjust the number of air filter devices according to the dust particle value and output the air filter device as the target device when the difference is the dust particle value.

[0071] It should be noted that: when the device provided in the above embodiment realizes its function, only the division of the above functional modules is used as an example. In actual application, the above functions can be assigned to different functional modules as needed, that is, the internal structure of the device is divided into different functional modules to complete all or part of the functions described above. In addition, the device and method embodiments provided in the above embodiment belong to the same concept, and the specific implementation process is detailed in the method embodiment, which will not be repeated here.

[0072] The present application also discloses an electronic device. Figure 3 , Figure 3 The electronic device 300 may include: at least one processor 301 , at least one network interface 304 , a user interface 303 , a memory 302 , and at least one communication bus 305 .

[0073] The communication bus 305 is used to realize the connection and communication between these components.

[0074] The user interface 303 may include a display screen (Display) and a camera (Camera). Optionally, the user interface 303 may also include a standard wired interface and a wireless interface.

[0075] The network interface 304 may optionally include a standard wired interface or a wireless interface (such as a WI-FI interface).

[0076] Among them, the processor 301 may include one or more processing cores. The processor 301 uses various interfaces and lines to connect various parts in the entire server, and executes various functions of the server and processes data by running or executing instructions, programs, code sets or instruction sets stored in the memory 302, and calling data stored in the memory 302. Optionally, the processor 301 can be implemented in at least one hardware form of digital signal processing (Digital Signal Processing, DSP), field programmable gate array (Field-Programmable Gate Array, FPGA), and programmable logic array (Programmable Logic Array, PLA). The processor 301 can integrate one or a combination of a central processing unit (Central Processing Unit, CPU), a graphics processing unit (Graphics Processing Unit, GPU) and a modem. Among them, the CPU mainly processes the operating system, user interface and application requests; the GPU is responsible for rendering and drawing the content to be displayed on the display screen; the modem is used to process wireless communications. It can be understood that the above-mentioned modem may not be integrated into the processor 301, and it can be implemented separately through a chip.

[0077] Among them, the memory 302 may include a random access memory (RAM) or a read-only memory (Read-Only Memory). Optionally, the memory 302 includes a non-transitory computer-readable storage medium. The memory 302 can be used to store instructions, programs, codes, code sets or instruction sets. The memory 302 may include a program storage area and a data storage area, wherein the program storage area. Instructions for implementing an operating system, instructions for at least one function (such as a touch function, a sound playback function, an image playback function, etc.), instructions for implementing the above-mentioned various method embodiments, etc. can be stored; the data storage area can store data involved in the above-mentioned various method embodiments, etc. The memory 302 can also be optionally at least one storage device located away from the aforementioned processor 301.

[0078] like Figure 3 As shown, the memory 302 as a computer storage medium may include an operating system, a network communication module, a user interface module, and an application program for clean room level processing.

[0079] exist Figure 3In the electronic device 300 shown, the user interface 303 is mainly used to provide an input interface for the user and obtain data input by the user; and the processor 301 can be used to call the application for clean room level processing stored in the memory 302. When executed by one or more processors, the electronic device executes one or more methods described in the above embodiments.

[0080] It should be noted that, for the aforementioned method embodiments, for the sake of simplicity, they are all described as a series of action combinations, but those skilled in the art should be aware that the present application is not limited by the order of the actions described, because according to the present application, certain steps can be performed in other orders or simultaneously. Secondly, those skilled in the art should also be aware that the embodiments described in the specification are all preferred embodiments, and the actions and modules involved are not necessarily required for the present application.

[0081] In the above embodiments, the description of each embodiment has its own emphasis. For parts that are not described in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0082] In the several embodiments provided in the present application, it should be understood that the disclosed devices can be implemented in other ways. For example, the device embodiments described above are only schematic, such as the division of the units, which is only a logical function division. There may be other division methods in actual implementation, such as multiple units or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be through some service interfaces, and the indirect coupling or communication connection of devices or units can be electrical or other forms.

[0083] The units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in one place or distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.

[0084] In addition, each functional unit in each embodiment of the present application may be integrated into one processing unit, or each unit may exist physically separately, or two or more units may be integrated into one unit. The above-mentioned integrated unit may be implemented in the form of hardware or in the form of software functional units.

[0085] If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable memory. Based on this understanding, the technical solution of the present application, or the part that contributes to the prior art, or all or part of the technical solution can be embodied in the form of a software product, which is stored in a memory and includes several instructions for a computer device (which can be a personal computer, server or network device, etc.) to execute all or part of the steps of the method described in each embodiment of the present application. The aforementioned memory includes: various media that can store program codes, such as USB flash drives, mobile hard drives, magnetic disks or optical disks.

[0086] The above is only an exemplary embodiment of the present disclosure and cannot be used to limit the scope of the present disclosure. That is, any equivalent changes and modifications made according to the teachings of the present disclosure are still within the scope of the present disclosure. After considering the disclosure of the specification and the truth of practice, it will be easy for those skilled in the art to think of other embodiments of the present disclosure. This application is intended to cover any variation, use or adaptive change of the present disclosure, which follows the general principles of the present disclosure and includes common knowledge or customary technical means in the technical field not recorded in the present disclosure.

Claims

1. A method for processing clean room level, characterized in that: Applied in a clean control platform, the method comprises: Responding to a purification request sent by a target person, the purification request is a request for adjusting the purification level of a target clean room, the target clean room being any operating room; determining a first purification level according to the purification request; Acquire first data corresponding to the target clean room; Determining, according to the first data, that the target clean room is currently at a second purification level; Determine a first value based on the first data, and determine a second value according to the first purification level; calculating a difference between the first value and the second value; The target device is adjusted according to the difference, so as to control the target clean room to be adjusted from the second purification level to the first purification level, and the target device is a device installed in the target clean room to perform air purification.

2. The method according to claim 1, characterized in that Determining, according to the first data, that the target clean room is currently at the second purification level specifically includes: Obtaining a first particle concentration value in the target clean room; Comparing the first particle concentration value with a preset standard threshold value to obtain a third purification level; Obtaining a third value, wherein the third value includes an air supply volume value, a pressure difference value, a temperature and humidity value, and a target gas concentration value; comparing the third value with a preset value corresponding to the third purification level; If the third value is consistent with the preset value, it is confirmed that the target clean room is currently in the third purification level, and the third purification level is output as the second purification level.

3. The method according to claim 1, characterized in that After adjusting the target equipment according to the difference so as to control the target clean room to be adjusted from the second purification level to the first purification level, the method further includes: Obtaining a first air supply volume value and a pressure difference value corresponding to the target clean room at a first moment; Determining whether the first air supply volume is within a preset air supply volume threshold, and whether the pressure difference value is within a preset pressure difference threshold, the first purification level including the preset air supply volume threshold and the preset pressure difference threshold; When the first air supply volume is within the preset air supply volume threshold, and the pressure difference value is within the preset pressure difference threshold, it is confirmed that the target device is in the first adjustment end state.

4. The method according to claim 3, characterized in that: After confirming that the target clean room is in the first adjustment end state when the first air supply volume is within the preset air supply volume threshold and the pressure difference value is within the preset pressure difference threshold, the method further includes: Obtaining a second particle concentration value and a temperature and humidity value corresponding to the target clean room at a second moment, where the second moment is after the first moment; Determine whether the second particle concentration value is within a preset particle concentration threshold, and whether the temperature and humidity values ​​are within a preset temperature and humidity threshold, the first purification level including the preset particle concentration threshold and the preset temperature and humidity threshold; When the second particle concentration value is within the preset particle concentration threshold, and the temperature and humidity values ​​are within the preset temperature and humidity threshold, confirming that the target device is in the second adjustment end state; According to the first adjustment end state and the second adjustment end state, it is determined that the target clean room is in an adjustment completion state, and the adjustment completion state indicates that the target device has adjusted the target clean room from the second purification level to the first purification level.

5. The method according to claim 4, characterized in that After determining whether the second particle concentration value is within a preset particle concentration threshold and whether the temperature and humidity values ​​are within a preset temperature and humidity threshold, the method further includes: When the second particle concentration value is not within the preset particle concentration threshold, and the temperature and humidity values ​​are not within the preset temperature and humidity thresholds, it is confirmed that the target device is in an adjustment unfinished state, and based on the adjustment unfinished state, it is determined that the target clean room is in an adjustment state.

6. The method according to claim 4, characterized in that After determining that the target clean room is in an adjustment completed state according to the first adjustment end state and the second adjustment end state, the method further includes: After confirming that the target clean room is at the first purification level, obtaining second data; Determining whether the second data is consistent with preset data; When the second data is inconsistent with the preset data, it is confirmed that the target clean room is in an abnormal state, and an early warning measure is determined according to the abnormal state.

7. The method according to claim 1, characterized in that The adjusting the target device according to the difference specifically includes: When the difference is an air volume value, the air supply device is adjusted according to the air volume value, and the air supply device is output as the target device; When the difference is a dust particle value, the number of air filter devices is adjusted according to the dust particle value, and the air filter devices are output as the target devices.

8. A clean room level processing device, characterized in that: The device is a clean control platform, comprising a receiving unit (201), a processing unit (202) and an adjustment unit (203); The receiving unit (201) is configured to respond to a purification request sent by a target person, the purification request being a request for adjusting the purification level of a target clean room, wherein the target clean room is any operating room; and obtain first data corresponding to the target clean room; The processing unit (202) determines a first purification level according to the purification request; determines that the target clean room is currently at a second purification level according to the first data; determines a first value based on the first data, and determines a second value according to the first purification level; and calculates a difference between the first value and the second value; The adjustment unit (203) adjusts the target device according to the difference so as to control the target clean room to be adjusted from the second purification level to the first purification level, wherein the target device is a device installed in the target clean room to perform air purification.

9. An electronic device, characterized in that: The electronic device (300) comprises a processor (301), a memory (302), a user interface (303) and a network interface (304), wherein the memory (302) is used to store instructions, the user interface (303) and the network interface (304) are used to communicate with other devices, and the processor (301) is used to execute the instructions stored in the memory (302) so that the electronic device (300) executes the method according to any one of claims 1 to 7.

10. A computer-readable storage medium, characterized in that: The computer-readable storage medium stores instructions, and when the instructions are executed, the method according to any one of claims 1 to 7 is executed.

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