Graphene wall surface application management method based on user immune requirement portrait

Abstract

The application discloses a graphene wall surface application management method based on user immune demand portrait and relates to the technical field of graphene wall surface application management, and comprises the following steps: collecting body temperature, skin resistance and microcirculation flow rate data of a user in an immune activity sudden drop stage, and constructing a dynamic monitoring sequence reflecting physiological fluctuation rhythm of the user on a time sequence; according to an immune activity real-time trend obtained in the dynamic monitoring sequence, performing time synchronization regulation on far infrared radiation power of a graphene wall surface, coordinating radiation rhythm in a high power output stage with an immune activity drop rate, and forming an adaptive slowing process of energy release. The application keeps far infrared radiation output and an immune state synchronous in the immune activity sudden drop stage, avoids heat stimulation mismatch through continuous smooth regulation, constructs a mild heat environment changing with an immune rhythm, reduces an immune burden and improves coordination between the environment and a physiological state of the human body.

Description

Technical Field

[0001] This invention relates to the field of graphene wall application management technology, specifically to a graphene wall application management method based on user immune demand profiles. Background Technology

[0002] Graphene wall application management refers to the intelligent operation and control of wall materials with the electrical, thermal, and far-infrared radiation properties of graphene in buildings or living spaces, covering the entire lifecycle and all parameters. Its core lies in collecting environmental indicators such as wall temperature, humidity, radiation intensity, and air ion concentration through sensor terminals, and combining this with the wall's own current, voltage, and heat distribution to dynamically manage the graphene wall's heating mode, energy output rhythm, and environmental regulation intensity, thereby achieving a balanced control of comfort, energy efficiency, and health benefits.

[0003] Graphene wall application management based on user immune demand profiles builds upon the above by introducing the concept of personalized immune health characteristic modeling. Specifically, it involves collecting users' physiological parameters (such as body temperature regulation characteristics, skin sensitivity, immune activity cycles, and circadian rhythms) and lifestyle data (such as sleep duration, exercise frequency, and residential climate characteristics) to create an immune demand profile. The system dynamically matches the graphene wall's operating mode based on this profile; for example, it increases far-infrared radiation to promote microcirculation during periods of low immune activity and reduces heat radiation intensity during periods of high stress to avoid immune burden, thereby achieving personalized and precise health environment intervention. This management model is essentially an adaptive environmental control process with the human immune status as the core feedback.

[0004] The existing technology has the following shortcomings: During periods of sudden drop in user immune activity, the graphene wall maintains high-power radiation output due to the lag in updating the immune profile, failing to adjust synchronously with the rapid changes in the user's physiological state. At this time, the far-infrared energy continuously released from the wall surface creates excessive heat stimulation in the local space, causing the user's microcirculation to remain in a state of prolonged hyperactivity. This abnormal heat stimulation can easily disrupt the body's immune homeostasis, causing immune cells to be in a state of continuous excitation or inhibition, disrupting the original immune regulatory rhythm. If this situation persists, it can easily lead to immune response disorders, resulting in problems such as fatigue-induced immunosuppression or reverse allergic reactions, not only affecting individual physiological comfort but also potentially exacerbating the underlying immune burden and causing health risks.

[0005] The information disclosed in the background section is only intended to enhance the understanding of the background of this disclosure, and therefore may include information that does not constitute prior art known to those skilled in the art. Summary of the Invention

[0006] The purpose of this invention is to provide a graphene wall application management method based on user immune demand profiles to solve the problems mentioned in the background art. To achieve the above objectives, the present invention provides the following technical solution: a graphene wall application management method based on user immune demand profiles, comprising the following steps:

[0007] Step 1: Collect data on the user's body temperature, skin resistance, and microcirculation velocity during the sudden drop in immune activity. Construct a dynamic monitoring sequence reflecting the user's physiological fluctuation rhythm on a time series basis to obtain real-time trend data on changes in immune activity, providing a continuous data foundation for subsequent adjustment of far-infrared radiation output. Step 2: Based on the real-time trend of immune activity obtained from the dynamic monitoring sequence, the far-infrared radiation power of the graphene wall is adjusted in time synchronization. The radiation rhythm of the high-power output stage is coordinated with the rate of decline of immune activity, forming an adaptive slowing process of energy release. The release rhythm of heat in the time dimension is controlled to suppress local heat accumulation. Step 3: During the energy release slowdown process, based on the current far-infrared radiation output state, the spatial distribution of local radiation hotspots on the wall is continuously rearranged. The radiation intensity ratio of each area is redistributed through time difference compensation, thereby achieving dynamic balance between the overheated and cooling areas in the spatial dimension and maintaining the stability of the microcirculation activity range. Step 4: Based on the dynamic equilibrium results of radiation intensity distribution, perform periodic corrections on the far-infrared radiation band, adjust the radiation power in the energy concentration area to the safe band range, so that the radiation intensity and immune rhythm remain synchronous and stable, and prevent abnormal physiological reactions caused by excessive heat stimulation. Step 5: Combining the periodic correction results of the far-infrared radiation band, the overall radiation output rhythm is continuously and smoothly regulated. The immune fluctuation rhythm reflected in the dynamic monitoring sequence is integrated with the energy release rhythm to construct a mild thermal environment that can automatically extend with the immune state, so as to achieve precise adaptive intervention for the stage of sudden drop in immune activity.

[0008] Preferably, the steps for collecting user data on body temperature, skin resistance, and microcirculation velocity during the immune activity drop phase include:

[0009] When the user enters the stage of sudden drop in immune activity, body temperature, skin resistance and microcirculation velocity are collected simultaneously. Body temperature collection focuses on changes in surface temperature, skin resistance collection is based on changes in skin conductance, and microcirculation velocity collection is based on changes in blood flow velocity in the superficial layer of the skin. The three types of data are collected at the same time interval and numbered with time stamps.

[0010] The collected data on continuous changes in body temperature, skin resistance, and microcirculation velocity are organized in chronological order, and the data sequences of different parameters are aligned under a unified time reference to form a multi-parameter joint monitoring sequence.

[0011] Based on the multi-parameter joint monitoring sequence, the correlation analysis of the changes in body temperature, skin resistance and microcirculation velocity over time was carried out to construct a dynamic monitoring sequence that reflects the user's physiological fluctuation rhythm.

[0012] Real-time trend information of immune activity changes is extracted from dynamic monitoring sequences. The combined changes in body temperature, skin resistance, and microcirculation velocity are correlated with the adjustment process of far-infrared radiation output to obtain a continuous data basis for immune activity changes.

[0013] Preferably, the step of performing time-synchronized adjustment of the far-infrared radiation power of the graphene wall surface based on the real-time trend of immune activity obtained from the dynamic monitoring sequence includes:

[0014] After obtaining the real-time trend of changes in immune activity in the dynamic monitoring sequence, the continuous change information representing the rate of decline in immune status is extracted and used as the basis for time adjustment of radiation power to determine the time reference benchmark for far-infrared radiation power adjustment.

[0015] Based on the rate of decline in immune activity, the temporal distribution of far-infrared radiation is synchronously adjusted. When the rate of decline in immune activity increases, the radiation power is gradually reduced, and when the rate of decline in immune activity is stable, a constant radiation output is maintained, thereby forming a time-synchronized control corresponding to the physiological fluctuation rhythm.

[0016] Based on the time-synchronized adjustment of far-infrared radiation power, adaptive slowing control is implemented on the energy release process. By gradually adjusting the rate of power change over a continuous period of time, a slowing process of heat release is achieved in the time dimension to prevent local heat accumulation.

[0017] During the adaptive slowdown of energy release, the rhythm of heat release is continuously controlled to ensure a smooth transition in radiative output power across different time periods. This maintains a moderate energy output during the decline in immune activity and gradually restores radiative power during the recovery of immune activity.

[0018] Preferably, in the step of continuously controlling the heat release rhythm during the adaptive slowdown process of energy release, the radiation output power is gradually adjusted according to the change in the rate of decline of immune activity in the time dimension, and the radiation power is gradually restored according to the time synchronization principle during the immune activity recovery stage, so that the far-infrared energy release process remains in a continuous and stable state in the time axis, thereby maintaining the stability of body surface temperature and the coordination of microcirculation activities during the immune activity fluctuation stage.

[0019] Preferably, during the energy release slowdown process, the step of continuously rearranging the spatial distribution of local radiation hotspots on the wall surface based on the current far-infrared radiation output state includes:

[0020] During the energy release slowdown process, based on the current far-infrared radiation output state, the radiation energy distribution data of different areas of the wall surface in the time dimension are obtained, and the radiation intensity, temperature change rate and energy output duration of each area are recorded to form thermal response characteristic data.

[0021] Based on thermal response characteristic data, the heat distribution status of different areas of the wall is identified, the location and heat intensity differences of local radiation hotspots and cooling zones are determined, and a local spatial radiation status distribution map is formed.

[0022] Based on the principle of time difference compensation, the proportion of radiation intensity in each region is redistributed. By delaying or advancing the duration of radiation output in each region, dynamic coordination of energy release is achieved in the time dimension.

[0023] Based on the redistribution of radiation intensity ratios in each region, the overall spatial heat distribution is continuously regulated. Spatial stability of energy distribution is maintained through balancing treatment, forming a dynamic equilibrium relationship between overheated and cooling zones in both time and space.

[0024] Preferably, in the process of continuously regulating the overall spatial heat distribution, the heat is kept fluid in the space by balancing the rate of change of radiation intensity in different regions. When a certain region shows a trend of heat accumulation, the energy release time of that region is delayed, so that the heat energy can diffuse to the adjacent regions. At the same time, the energy gradient change between adjacent regions is controlled on the basis of time synchronization, so as to maintain the temperature difference within a stable range.

[0025] Preferably, the step of performing periodic correction on the far-infrared radiation band based on the dynamic equilibrium result of the radiation intensity distribution includes:

[0026] After obtaining the dynamic equilibrium result of the radiation intensity distribution, the current far-infrared radiation output state is periodically identified to determine the energy release cycle and radiation frequency distribution characteristics of different regions, and the radiation cycle of the energy concentration area is time-correlated with the immune activity rhythm.

[0027] Based on the radiation output characteristics of the energy concentration area, the far-infrared radiation band is mapped to form a time and space distribution map of the radiation band, and the bands that exceed the safe absorption range of the human body are identified and calibrated.

[0028] Based on the band mapping results, the radiation power in the energy concentration area is periodically corrected. By extending the radiation period or reducing the radiation peak value, the power output is adjusted to form a flexible transition of energy release within the safe band range.

[0029] Based on the periodic correction of radiation power in the energy concentration area, rhythm matching control is performed on the overall far-infrared radiation band. The radiation output frequency is dynamically matched according to the periodic characteristics of immune activity changes, so that the radiation intensity and immune rhythm maintain a synchronous and stable relationship.

[0030] Preferably, during the rhythm matching control process, the modified far-infrared radiation band is continuously adjusted in the time dimension according to the periodic characteristics of immune activity changes. When immune activity is in the declining phase, the radiation power is kept in a mild range. When immune activity is in the recovery phase, the radiation power gradually increases. When immune activity is in the stable phase, the radiation power is kept constant to maintain the synchronous and stable relationship between radiation intensity and immune rhythm.

[0031] Preferably, the steps for continuously and smoothly controlling the overall radiation output rhythm, based on the periodic correction results of the far-infrared radiation band, include:

[0032] After obtaining the periodic correction results of the far-infrared radiation band, the variation law of the corrected radiation output in the time dimension is collected to determine the initial state of the overall radiation output rhythm and form a basic sequence reflecting the periodic changes in energy release.

[0033] The collected radiation output rhythm is fused with the immune fluctuation rhythm reflected in the dynamic monitoring sequence to establish a matching relationship between energy release and immune status on the time axis, so that the change in radiation output rhythm and immune fluctuation rhythm form a dynamic correspondence.

[0034] Based on the integration of immune fluctuation rhythm and radiation output rhythm, the overall radiation output rhythm is continuously and smoothly regulated. By adjusting the energy release time interval and rate of change, the stability and continuity of the heat energy output process are maintained.

[0035] Based on the correspondence between the fused radiation output rhythm and the immune fluctuation rhythm, the overall thermal environment is gently regulated to maintain a synchronous and stable relationship between the far-infrared radiation output intensity and the immune state, thereby constructing a mild thermal environment that can automatically extend with the immune state.

[0036] Preferably, in the step of continuously and smoothly regulating the overall radiation output rhythm, the rate of change of radiation power is smoothly transitioned between adjacent time periods by extending the time interval. During the energy release process, the energy release interval is extended when the radiation output rate increases and shortened when the radiation output rate decreases, so as to maintain the continuity of the heat energy output process and keep the immune fluctuation rhythm and energy release rhythm dynamically consistent.

[0037] The technical effects and advantages provided by the present invention in the above technical solution are as follows:

[0038] This invention introduces a dynamic monitoring sequence-based regulation mechanism during the immune activity drop phase, enabling far-infrared radiation output to remain synchronized with changes in the user's immune status, thereby avoiding temporal and spatial mismatch in radiation power. Through continuous regulation of radiation power, radiation rhythm, and radiation band, the heat release process transforms from a rigid output to a flexible output that gradually extends with changes in immune rhythm, keeping the body's surface microcirculation activity within a stable range. This effectively reduces the interference of local heat stimulation on the body's immune homeostasis, reduces the physiological burden caused by concentrated energy, and allows users to remain in a comfortable and harmonious thermal environment even during periods of fluctuating immune activity, thus improving the overall compatibility between the living environment and the body's physiological state.

[0039] This invention deeply integrates the rhythm of immune fluctuations with the rhythm of energy release, constructing a mild thermal environment regulation method that automatically extends with the immune state. This transforms environmental intervention from simple temperature control into an adaptive regulatory process centered on the human immune state. This method can smoothly adjust radiation output during periods of decreased immune activity and naturally connect with changes in energy release during the recovery process, avoiding the impact of sudden changes in radiation intensity on the physiological system and thus reducing the probability of immune response disorders. Through this continuous and smooth regulation process, not only is the precision of environmental regulation improved, but long-term use also helps to reduce potential immune burden and enhance the stability and sustainability of health environment interventions. Attached Figure Description

[0040] To more clearly illustrate the technical solutions in the embodiments of this application or the prior art, the drawings used in the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments recorded in this invention. For those skilled in the art, other drawings can be obtained based on these drawings.

[0041] Figure 1 This is a flowchart of the graphene wall application management method based on user immune demand profiles according to the present invention. Detailed Implementation

[0042] Exemplary embodiments will now be described more fully with reference to the accompanying drawings. However, these exemplary embodiments can be implemented in many forms and should not be construed as limited to the examples set forth herein; rather, they are provided so that the description of this disclosure will be more complete and fully convey the concept of the exemplary embodiments to those skilled in the art.

[0043] This invention provides, for example Figure 1 The graphene wall application management method shown, based on user immune demand profiles, includes the following steps:

[0044] Step 1: Collect data on the user's body temperature, skin resistance, and microcirculation velocity during the sudden drop in immune activity. Construct a dynamic monitoring sequence reflecting the user's physiological fluctuation rhythm on a time series basis to obtain real-time trend data on changes in immune activity, providing a continuous data foundation for subsequent adjustment of far-infrared radiation output. The specific implementation method for this step is as follows:

[0045] When a user enters the phase of a sudden drop in immune activity, body temperature, skin resistance, and microcirculation velocity are simultaneously collected. Body temperature collection focuses on changes in the user's surface temperature, continuously recording data at different time points to reflect the dynamic state of metabolic responses. Skin resistance collection is based on changes in the electrical conductivity of the skin surface, continuously detecting changes in the electrical signal to reflect fluctuations in skin moisture content and ion concentration, thus indirectly reflecting the sensitivity of physiological responses on the skin surface. Microcirculation velocity collection records changes in the velocity of superficial blood flow to reflect the patency of peripheral blood vessels and the continuity of blood flow. During this process, all three types of data are collected at equal time intervals and numbered using a time stamp to ensure that body temperature, skin resistance, and microcirculation velocity form comparable, continuous records under the same time frame. This continuous collection allows for a complete reflection of the dynamic physiological changes at the user's body surface and microcirculation levels during the period of decreased immune activity.

[0046] After collecting continuous data on changes in body temperature, skin resistance, and microcirculation velocity, the data is organized chronologically. Specifically, the collected body temperature, skin resistance, and microcirculation velocity data sequences are arranged at uniform time intervals, ensuring complete correspondence between the sampling times of different parameters. This time-synchronized organization ensures that each data point matches the other two physiological parameters at the same time point, accurately reflecting the overall physiological state at that moment in subsequent analysis. In this process, a baseline time axis for sampling is first determined, and various data are archived using timestamps. Then, data segments with time deviations are interpolated or time-registered to maintain strict alignment in the time dimension. Finally, the three types of data are arranged chronologically to form a multi-parameter joint monitoring sequence. This joint monitoring sequence integrates the thermal response characteristics of body temperature, the electrical response characteristics of skin resistance, and the blood flow characteristics of microcirculation velocity in a temporal manner, thus forming a continuous and complete record of physiological changes on the time axis.

[0047] After obtaining the multi-parameter joint monitoring sequence, correlation analysis is performed on the continuous changes of each physiological parameter over time to construct a dynamic monitoring sequence reflecting the user's physiological rhythm. In this process, the curves of body temperature change over time, skin resistance change over time, and microcirculation velocity change over time are compared according to time nodes, ensuring that the data at each time point corresponds to a specific physiological state. For example, when body temperature rises continuously in a short period, the decrease in skin resistance and the increase in microcirculation velocity usually correspond to a physiological response state of accelerated peripheral circulation. By continuously comparing these relationships, the fluctuation characteristics of different physiological parameters over time can be systematically linked to form a continuous monitoring sequence that reflects changes in the user's physiological rhythm. This dynamic monitoring sequence is continuous in time and integrates the changing trends of multiple physiological parameters, thus possessing the ability to track changes in immune activity over time. This sequence not only reflects the overall physiological trend of the user during the decline in immune activity but also demonstrates the interaction relationships between different physiological parameters, such as the correspondence between rising body temperature and decreasing skin resistance, and the correlation between changes in microcirculation velocity and fluctuations in body surface temperature. This multi-parameter correlation method enables dynamic monitoring sequences to accurately depict the physiological fluctuation rhythms during the decline of immune activity over time.

[0048] After the dynamic monitoring sequence is constructed, real-time trend information reflecting changes in immune activity is extracted from the sequence and used as the continuous data basis for adjusting far-infrared radiation output. Specifically, the trend of immune activity is first determined based on the combined changes in body temperature, skin resistance, and microcirculation velocity over time. When the fluctuation range of body temperature decreases, skin resistance remains stable, and microcirculation velocity decreases, it usually indicates that immune activity is in a downward phase. By continuously tracking this trend, dynamic information on the rate and duration of the decline in immune activity can be obtained in real time. Subsequently, the extracted trend information is integrated with the far-infrared radiation control system to ensure that the changes in far-infrared radiation power output from the wall are consistent with the downward trend of the user's immune activity over time, thereby coordinating the rhythm of energy output with the physiological state. Through the real-time correlation between trend information and radiation control, far-infrared radiation output can form a gradual energy release during the sudden drop in immune activity, avoiding excessive heat accumulation in local areas. As the dynamic monitoring sequence is updated in real time, the trend of immune activity changes is also updated, ensuring that the output rhythm of far-infrared radiation is always coordinated with the user's physiological state, forming a continuous control process centered on physiological feedback.

[0049] Through the implementation of the above process, the continuous changes in user body temperature, skin resistance, and microcirculation velocity are accurately recorded and integrated into a unified time series, forming a dynamic monitoring sequence reflecting the changing trend of immune activity. The output of this monitoring sequence provides continuous data input for subsequent adjustment of far-infrared radiation power, enabling the graphene wall surface to adjust the radiation output rhythm according to the user's real-time physiological state during the immune activity drop phase. This achieves dynamic adaptation of far-infrared energy release in both time and energy dimensions, providing the user with a mild thermal environment that changes synchronously with their immune state, avoiding the accumulation of immune burden caused by continuous heat stimulation, and maintaining the stability of environmental regulation and physiological coordination.

[0050] Step 2: Based on the real-time trend of immune activity obtained from the dynamic monitoring sequence, the far-infrared radiation power of the graphene wall is adjusted in time synchronization. The radiation rhythm of the high-power output stage is coordinated with the rate of decline of immune activity, forming an adaptive slowing process of energy release. The release rhythm of heat in the time dimension is controlled to suppress local heat accumulation.

[0051] The specific implementation method for this step is as follows:

[0052] After obtaining the real-time trend of immune activity changes reflected in the dynamic monitoring sequence, continuous change information representing the rate of decline in immune status is extracted and used as the basis for time-based adjustment of radiation power. The change in the real-time trend of immune activity reflects the time-dependent relationship between the user's physiological load and body temperature response. Therefore, at this stage, a time reference benchmark for power adjustment needs to be established based on the fluctuation amplitude and rate of decline of this trend. By continuously monitoring the rate of decline in immune activity, the duration of the transition phase from a high to a low immune status can be determined, and the synchronization starting point for far-infrared radiation power adjustment can be determined accordingly. At this point, power adjustment is not an instantaneous switch, but rather a gradual guidance of energy output according to the rate of change in immune activity, keeping the energy release process synchronized with the physiological change process. Thus, in the initial stage of a sudden drop in immune activity, the radiation power of the graphene wall will not immediately decrease significantly, but will be gradually adjusted according to the rhythm of the decline in immune status, allowing the energy output rhythm to transition naturally.

[0053] After determining the time reference for adjusting radiation power, the temporal distribution of far-infrared radiation is synchronously adjusted according to the rate of decline in immune activity. During this phase, changes in power output follow a time-delay principle: the adjustment range of radiation power is relatively larger during periods of rapid decline in immune activity, and relatively slower during periods of slow decline. This time-delay-based synchronous adjustment ensures that the curve of far-infrared energy release is coordinated with the curve of immune activity change. Specifically, when the rate of decline in immune activity continues to increase, the far-infrared radiation power gradually decreases to prevent a rapid increase in the user's body surface temperature; when the rate of decline in immune activity tends to stabilize, the radiation power remains relatively constant to maintain the thermal balance of the physiological environment. Throughout this process, the time interval of power adjustment is consistent with the temporal resolution of immune activity changes, ensuring that changes in energy output closely correspond to the physiological fluctuation rhythm, thus achieving synchronous dynamic control in the time dimension.

[0054] After the far-infrared radiation power is adjusted in time synchronization, the energy release process is further adaptively slowed down to achieve a smooth transition in heat release. In this stage, power changes are not targeted at a single numerical adjustment, but rather by gradually controlling the rate of power change over a continuous period, allowing energy release to form a continuous, gradual decrease over time. This prevents heat accumulation in localized areas due to concentrated radiation energy. Specifically, when the downward trend in immune activity continues, the far-infrared radiation power gradually decreases in each sampling cycle, ensuring that the gradient of power output change aligns with the gradient of the decrease in immune activity. Through continuous gradual adjustment, heat from the wall surface is released in a dispersed manner over time, achieving adaptive slowing of energy distribution. This slowing process not only reduces surface stimulation caused by instantaneous heat concentration but also creates a balanced state in the heat release rhythm, maintaining physiological comfort for the user during the decline in immune activity while avoiding interference with microcirculation due to heat load.

[0055] Finally, during the adaptive slowdown of energy release, the rhythm of heat release over time is continuously controlled to maintain the stability and coordination of the entire energy output process. Building upon the previous stage, this phase utilizes the achieved slow-deceleration output characteristics to continuously optimize the time intervals and rhythms of heat release, ensuring a continuous connection between radiative output power across different time periods. When immune activity declines to a low level, the radiative output power is maintained within a relatively mild energy range to prevent localized heat accumulation and subsequent expansion of the body's microcirculation. As immune activity begins to recover, the radiative power gradually recovers according to the principle of time synchronization, thus establishing a positive response relationship between immune status and energy output. Through this continuous temporal rhythm control, the far-infrared radiative power remains synchronized and coordinated with the user's physiological changes throughout the entire immune activity fluctuation process, enabling energy output to form an adaptive regulatory closed loop over time. This process results in a more balanced temporal distribution of heat release, effectively suppressing localized temperature rises and maintaining stable body surface temperature changes, thereby maintaining the normal flow rhythm of microcirculation and reducing the physiological burden during the immune system's sudden drop phase.

[0056] By implementing the above steps, the temporal variation of far-infrared radiation power can be synchronized with the rate of decline in immune activity, forming a continuous, coordinated, and smooth time control mechanism during energy output. This mechanism achieves adaptive slowing of energy release, dispersing heat release over time, avoiding excessive stimulation caused by localized heat accumulation, and maintaining a stable relationship between the user's body surface temperature and physiological response during periods of decreased immune activity. Therefore, the far-infrared radiation output process of the graphene wall is no longer a simple temperature control behavior, but a time-synchronized adjustment process based on immune activity trends, ensuring that the energy release rhythm is coordinated with the human immune state, thus forming a physiologically adaptive thermal environment control mode during periods of sudden decline in immune activity.

[0057] Step 3: During the energy release slowdown process, based on the current far-infrared radiation output state, the spatial distribution of local radiation hotspots on the wall is continuously rearranged. The radiation intensity ratio of each area is redistributed through time difference compensation, thereby achieving dynamic balance between the overheated and cooling areas in the spatial dimension and maintaining the stability of the microcirculation activity range.

[0058] The specific implementation method for this step is as follows:

[0059] During the energy release slowdown process, data on the distribution of radiant energy across different areas of the wall surface over time is acquired based on the current far-infrared radiation output state. The far-infrared radiation output state includes the radiation intensity, temperature change rate, and energy output duration of each local area within each time period during the energy slowdown phase. Continuous acquisition of data from these time periods allows for the acquisition of the thermal response characteristics of different areas of the wall surface during the energy release process. The main objective of this stage is to clarify the spatial distribution differences in the current far-infrared radiation output and identify localized high-energy and relatively low-energy areas formed due to adjustments in the energy output rhythm. Because power adjustments have a time-dependent effect during the energy release slowdown process, and different areas exhibit varying energy response rates, the radiation intensity across different areas of the wall surface is often uneven at any given moment. Continuously recording this spatial thermal distribution information provides fundamental data support for subsequent identification of radiation hotspots and energy rearrangement.

[0060] After acquiring the current far-infrared radiation output status, the heat distribution status of different areas of the wall is identified to determine the location of local radiation hotspots and cooling zones, as well as their relative heat intensity differences. During this stage, by continuously comparing the radiation intensity change trends of different areas, it is determined which areas are in a high-radiation state and which are in an energy-deficient state. When the radiation output of a high-energy area consistently exceeds the heat release level of adjacent areas, that area is considered a local radiation hotspot; while areas with relatively low energy output and slow temperature changes are considered relatively cooling zones. In this identification process, considering the temporal continuity of the energy release slowdown phase, the determination of hotspots and cooling zones is based on continuous temporal changes, rather than single-moment data, thus ensuring that the identified hotspot distribution accurately reflects the spatial energy accumulation trend. At this point, the location, area, and heat accumulation rate of the hotspot areas are recorded, forming a distribution map of the local spatial radiation status, providing a basis for subsequent energy redistribution.

[0061] After identifying local radiation hotspots and cooling zones, the radiation intensity ratio of each area is redistributed according to the principle of time difference compensation. In this stage, by comparing the radiation output state of different areas in the previous time period, the time difference characteristics of energy release are determined, and the energy rebalancing is achieved by delaying or advancing the duration of radiation output in each area. Specifically, when an area was in a state of sustained high radiation in the previous time period, while adjacent areas had lower energy output, the energy release rhythm of the high-radiation area is appropriately slowed down in the current time period, causing a slight delay in its heat output. This allows the cooling zone to receive relatively compensatory heating to balance the overall heat distribution. Simultaneously, for areas with insufficient energy output in the previous time period, the energy release duration is appropriately extended in the current stage to provide additional heat compensation, achieving dynamic coordination of energy release between different spatial areas. Through this time difference compensation method, the wall surface forms an alternating heat output rhythm during energy release, preventing energy from remaining in local spaces for extended periods, thus achieving heat diffusion and dispersion in both time and space dimensions.

[0062] After the radiant intensity ratios of each region are redistributed, the overall spatial heat distribution is continuously regulated to maintain a dynamic equilibrium between overheated and cooling zones on the wall surface during the energy release slowdown phase. The key to this stage is maintaining spatial stability of the energy distribution, preventing sustained heat concentration in localized areas as time progresses. To achieve this, based on the redistribution results from the previous stage, the rate of change of radiant intensity in different regions is balanced, ensuring heat mobility within the space. If a region still shows a tendency to accumulate heat after energy output adjustments, its subsequent energy release is slightly delayed, allowing heat to diffuse to surrounding areas, thus achieving spatial thermal equilibrium. Furthermore, to prevent excessive temperature rise in the cooling zone after continuous compensation heating, the system controls the energy gradient changes between adjacent regions based on time synchronization, maintaining the temperature difference within a stable range. Through this continuous spatial distribution balance regulation, the wall surface forms a dynamic and balanced heat distribution state during the energy release process, so that heat energy is transferred between different areas in a stable manner, thereby ensuring that the far-infrared radiation intensity in the user's space remains coordinated, avoiding continuous heat stimulation or excessive energy accumulation in local areas, and ensuring that the microcirculation activity range remains stable in time and space.

[0063] Through the above steps, the spatial distribution of local radiation hotspots on the wall surface can be continuously rearranged based on the current far-infrared radiation output state during the energy release slowdown process. Furthermore, the radiation intensity ratio of each area is redistributed through time difference compensation, thereby achieving dynamic equilibrium of heat distribution in the spatial dimension and preventing the formation of overheated zones and energy concentration. This process ensures coordinated changes in far-infrared radiation output within the spatial range, forming a time- and space-synchronized energy release mechanism. This maintains a stable microcirculation activity range, preventing abnormal local physiological responses caused by uneven heat distribution, and providing a stable spatial thermal balance basis for subsequent radiation band periodic correction and overall rhythm smoothing control.

[0064] Step 4: Based on the dynamic equilibrium results of radiation intensity distribution, perform periodic corrections on the far-infrared radiation band, adjust the radiation power in the energy concentration area to the safe band range, so that the radiation intensity and immune rhythm remain synchronous and stable, and prevent abnormal physiological reactions caused by excessive heat stimulation.

[0065] The specific implementation method for this step is as follows:

[0066] After obtaining the dynamic equilibrium results of the radiation intensity distribution, the current far-infrared radiation output state is periodically identified to determine the energy release cycle and radiation frequency distribution characteristics of different regions. The identification of the radiation cycle is based on the fluctuation pattern of energy output over time. By analyzing the changing trend of radiation intensity in each region over a continuous time period, the duration and frequency variation range of radiation output in the energy concentration area are determined. After the dynamic equilibrium of energy distribution, although thermal rebalancing has been achieved at the spatial level, some regions may still experience overlapping radiation cycles or uneven energy output cycles over time, causing the same region to be in a high-energy radiation state multiple times within a short period. By identifying the radiation output cycle, the fluctuation pattern of the energy concentration area in different time periods can be clarified, providing a time reference for subsequent band adjustments. At this point, each energy release cycle corresponds temporally to the rhythm of changes in immune activity, thus ensuring that the subsequent adjustment process can be coordinated with physiological rhythms in time.

[0067] After completing the radiation cycle identification, the far-infrared radiation bands are mapped based on the radiation output characteristics of the energy concentration areas to determine whether the current output band is within the safe absorption range of the human body. This stage involves overlaying the dynamically balanced spatial distribution results with the time cycle identification results, combining the temporal energy release frequency and spatial energy concentration of each region to form a temporal-spatial distribution map of the radiation bands. In this distribution map, energy concentration areas typically exhibit a dense band distribution and a high frequency range, easily leading to local heat accumulation and prolonged thermal load on the skin surface. When this high-frequency radiation state overlaps with a phase of decreased immune activity, it can easily produce an excessive heat stimulation effect, interfering with the balance of the immune system. Therefore, in this stage, the radiation bands of each energy concentration area are mapped to a preset safe band range, and bands exceeding the safe absorption range of the human body are identified and calibrated. Through this mapping process, it is possible to determine which radiation outputs require adjustment in both temporal and spatial dimensions, thus providing a basis for subsequent energy correction.

[0068] After band mapping is completed, the radiation power of the energy concentration area is periodically corrected based on the mapping results to keep the radiation output of each region within a safe band range. In this stage, the power output of identified high-frequency bands or high-intensity radiation areas is gradually adjusted over time by extending the radiation period or reducing the radiation peak value, thus gradually converging the energy release curve towards a safe range. Simultaneously, for some areas in the low-energy or cooling zones, their radiation power is appropriately increased to maintain a balanced overall band distribution across the spectrum, resulting in a periodic alternation of energy output. During this process, the power adjustment of the energy concentration area is synchronized with the changing trend of immune activity. When immune activity is low, the radiation power decreases to a band range suitable for human absorption; as immune activity gradually recovers, the radiation power rises back to a stable output range. Through this periodic power correction, the radiation output of the energy concentration area achieves a flexible transition over time, forming a safe boundary within the band range and effectively preventing the continuous accumulation of excessive heat stimulation.

[0069] After the radiation power in the energy concentration zone is periodically corrected, rhythm-matching control is implemented on the overall far-infrared radiation band to maintain a stable synchronous relationship between radiation intensity and immune rhythm. During this stage, based on the cyclical characteristics of immune activity changes, the corrected radiation band is dynamically correlated with the immune fluctuation rhythm, ensuring that the energy release rhythm of far-infrared radiation is synchronously coupled with the response cycle of the human immune system. When the immune rhythm enters the recovery phase, the radiation output band remains in a mild range to promote microcirculation balance; when the immune rhythm is in a stable phase, the radiation band maintains a constant output to maintain the balance between body surface temperature and blood flow; when the immune rhythm re-enters a low-activity phase, the radiation output cycle automatically adjusts to a low-power range to avoid excessive heat stimulation that could trigger physiological abnormalities. Through this rhythm-matching control, the output frequency of far-infrared radiation is synchronized with the immune fluctuation cycle, making the energy release process continuous and adaptive. At this time, the adjustment of the radiation band not only ensures the safety of heat output but also creates a coordinated feedback between heat distribution and immune activity, thereby preventing localized heat accumulation that could cause abnormalities in the body surface microcirculation and maintaining the stability of the body's physiological rhythm.

[0070] Through the implementation of the above steps, based on the dynamic equilibrium results of radiation intensity distribution, the periodic correction of the far-infrared radiation band is completed, effectively adjusting the radiation power in the energy concentration area to within the safe band range, thus avoiding the heat stress effect caused by the long-term overheating of high-energy areas. This process forms a coordinated energy control mechanism in both time and space, maintaining a synchronous and stable relationship between radiation output and immune rhythm, ensuring that the physiological stimulation of far-infrared radiation is within an appropriate range, and preventing heat accumulation on the body surface, microcirculatory imbalance, and immune rhythm disorder caused by excessive energy output. This achieves dual stability of temperature control and immune balance during the sudden drop in immune activity.

[0071] Step 5: Combining the periodic correction results of the far-infrared radiation band, the overall radiation output rhythm is continuously and smoothly regulated. The immune fluctuation rhythm reflected in the dynamic monitoring sequence is integrated with the energy release rhythm to construct a mild thermal environment that can automatically extend with the immune state, so as to achieve precise adaptive intervention for the stage of sudden drop in immune activity.

[0072] The specific implementation method for this step is as follows:

[0073] After obtaining the periodic correction results for the far-infrared radiation band, the temporal variation of the corrected radiation output is collected to determine the initial state of the overall radiation output rhythm. Radiation output rhythm refers to the intensity variation trajectory and frequency distribution of far-infrared energy release over a continuous time period, reflecting the dynamic change process of wall surface heat release over time. After periodic correction, the radiation power in the energy concentration area has been adjusted to a safe band, but differences in energy release rhythm still exist between time periods. Therefore, during this stage, the radiation intensity, power change rate, and heat release duration are continuously collected in different time slices, ensuring that the energy output characteristics of each time period correspond to the correction state of the previous stage. Through this rhythm acquisition process, a basic sequence reflecting the periodic changes in energy release can be obtained, providing a temporal reference for subsequent integration with the immune fluctuation rhythm. At this point, the acquired radiation rhythm not only contains power change information but also the temporal distribution pattern during the energy release process, thus providing a complete description of the corrected energy dynamic state.

[0074] After collecting the overall radiation output rhythm, this rhythm is fused with the immune fluctuation rhythm reflected in the dynamic monitoring sequence to establish a temporal matching relationship between energy release and immune status. The immune fluctuation rhythm originates from the user's physiological monitoring results during the sudden drop in immune activity, reflecting the continuous changing trends of body temperature, skin resistance, and microcirculation velocity over time. By mapping this rhythm one-to-one with the radiation output rhythm on the time axis, a coordinated match is achieved between the two in terms of fluctuation period, response delay, and amplitude. When the immune fluctuation rhythm shows a downward trend, the radiation output rhythm correspondingly reduces the energy release rate; when the immune fluctuation rhythm shows an upward trend, the radiation output rhythm gradually restores the energy output intensity. In this fusion process, the changes in the radiation output rhythm are not adjusted to a fixed value, but rather achieve a continuous and flexible transition based on the periodic changes of the immune fluctuation rhythm, ensuring that the heat energy release remains dynamically consistent with physiological fluctuations in the time dimension. Through this rhythm fusion, the changing trend of the immune status directly affects the temporal control of energy release, thereby establishing a heat energy coordination mechanism driven by immune feedback.

[0075] After integrating the immune fluctuation rhythm with the radiation output rhythm, the overall radiation output rhythm is continuously and smoothly regulated to eliminate any abrupt or discontinuous changes that may occur during energy release, maintaining the continuity and stability of the heat output process. In this stage, by extending the energy change intervals between time segments, the rate of change in radiation power is made to transition smoothly between adjacent time periods. When radiation output shows a rapid increase in energy over a short period, the instantaneous rate of change is reduced by extending the energy release interval; when radiation output continuously decreases over a certain period, the interval is shortened to maintain a stable heat output level. Through this continuous and smooth regulation, the radiation output rhythm maintains a stable fluctuation curve across the entire time axis, avoiding drastic fluctuations in body surface temperature due to excessively rapid energy changes. Simultaneously, during the smooth regulation process, the trend of radiation rhythm changes still corresponds to the immune fluctuation rhythm, allowing users to experience a stable and balanced thermal environment during periods of sudden drop in immune activity. This continuous temporal smoothing control ensures a predictable and adjustable continuous response relationship between the energy release rhythm and changes in immune status.

[0076] After completing continuous smooth regulation, the overall thermal environment is gently adjusted based on the correspondence between the fused radiation output rhythm and the immune fluctuation rhythm. This ensures that the intensity of radiation output maintains a stable and synchronous relationship with the human immune state, creating a mild thermal environment that automatically extends with the immune state. During this stage, the stable range of far-infrared radiation output is determined by integrating the aforementioned time-smoothing regulation results with the trend of immune rhythm changes. When immune activity is declining, radiation output remains within the mild range, coordinating the energy release rate with the rate of immune decline to avoid heat accumulation and surface irritation. When immune activity is stable, radiation output maintains a stable release to maintain continuous microcirculation. As immune activity gradually recovers, radiation output increases slowly, ensuring positive synchronization between energy release and immune recovery rates. Through this gentle regulation process, the energy output rhythm of the entire thermal environment can automatically extend according to changes in the user's immune state, forming a continuous, flexible, and adaptive far-infrared radiation regulation mechanism. Ultimately, the wall surface achieves an adaptive thermal equilibrium over time, allowing users experiencing a sudden drop in immune activity to receive thermal stimulation in a thermal environment that matches their physiological rhythm, avoiding the immune burden caused by excessive radiation, while simultaneously promoting stable microcirculation and the natural recovery of immune function.

[0077] Through the continuous execution of the above steps, combined with the periodic correction results of the far-infrared radiation band, the overall radiation output rhythm is continuously and smoothly regulated. This integrates the immune fluctuation rhythm reflected in the dynamic monitoring sequence with the energy release rhythm, thereby forming a mild thermal environment that can automatically extend with the immune state. This process, through the smooth control of energy output in the time dimension and the dynamic matching of immune rhythm in the physiological dimension, ensures that the release rhythm of far-infrared radiation remains coordinated with the human immune state. This ensures that during the phase of sudden drop in immune activity, the thermal energy output can both maintain the temperature stability of the environment and achieve precise adaptive intervention to the human immune function, achieving a balance between energy saving, comfort, and health.

[0078] Beneficial effect 1:

[0079] This invention introduces a dynamic monitoring sequence-based regulation mechanism during the immune activity drop phase, enabling far-infrared radiation output to remain synchronized with changes in the user's immune status, thereby avoiding temporal and spatial mismatch in radiation power. Through continuous regulation of radiation power, radiation rhythm, and radiation band, the heat release process transforms from a rigid output to a flexible output that gradually extends with changes in immune rhythm, keeping the body's surface microcirculation activity within a stable range. This effectively reduces the interference of local heat stimulation on the body's immune homeostasis, reduces the physiological burden caused by concentrated energy, and allows users to remain in a comfortable and harmonious thermal environment even during periods of fluctuating immune activity, thus improving the overall compatibility between the living environment and the body's physiological state.

[0080] Benefit 2:

[0081] This invention deeply integrates the rhythm of immune fluctuations with the rhythm of energy release, constructing a mild thermal environment regulation method that automatically extends with the immune state. This transforms environmental intervention from simple temperature control into an adaptive regulatory process centered on the human immune state. This method can smoothly adjust radiation output during periods of decreased immune activity and naturally connect with changes in energy release during the recovery process, avoiding the impact of sudden changes in radiation intensity on the physiological system and thus reducing the probability of immune response disorders. Through this continuous and smooth regulation process, not only is the precision of environmental regulation improved, but long-term use also helps to reduce potential immune burden and enhance the stability and sustainability of health environment interventions.

[0082] The foregoing has only described certain exemplary embodiments of the present invention by way of illustration. Undoubtedly, those skilled in the art can modify the described embodiments in various ways without departing from the spirit and scope of the present invention. Therefore, the foregoing drawings and descriptions are illustrative in nature and should not be construed as limiting the scope of protection of the claims of the present invention.

Claims

1. A graphene wall application management method based on user immune demand profiles, characterized in that, Includes the following steps: Step 1: Collect data on body temperature, skin resistance, and microcirculation velocity of the user during the immune activity drop phase, and construct a dynamic monitoring sequence reflecting the user's physiological fluctuation rhythm on a time series basis. Step 2: Based on the real-time trend of immune activity obtained from the dynamic monitoring sequence, the far-infrared radiation power of the graphene wall is adjusted in time synchronization to coordinate the radiation rhythm of the high-power output stage with the rate of decline of immune activity, forming an adaptive slowing process of energy release. Step 3: During the energy release slowdown process, based on the current far-infrared radiation output state, the spatial distribution of local radiation hotspots on the wall is continuously rearranged, and the radiation intensity ratio of each area is redistributed through time difference compensation. Step 4: Based on the dynamic equilibrium results of the radiation intensity distribution, perform periodic corrections on the far-infrared radiation band to adjust the radiation power in the energy concentration area to the safe band range. Step 5: Combining the periodic correction results of the far-infrared radiation band, the overall radiation output rhythm is continuously and smoothly regulated. The immune fluctuation rhythm reflected in the dynamic monitoring sequence is integrated with the energy release rhythm to construct a mild thermal environment that can automatically extend with the immune status.

2. The graphene wall application management method based on user immune demand profiles according to claim 1, characterized in that, The steps for collecting user data on body temperature, skin resistance, and microcirculation velocity during the immune activity drop phase include: When the user enters the stage of sudden drop in immune activity, body temperature, skin resistance and microcirculation velocity are collected simultaneously. Body temperature collection focuses on changes in surface temperature, skin resistance collection is based on changes in skin conductance, and microcirculation velocity collection is based on changes in blood flow velocity in the superficial layer of the skin. The three types of data are collected at the same time interval and numbered with time stamps. The collected data on continuous changes in body temperature, skin resistance, and microcirculation velocity are organized in chronological order, and the data sequences of different parameters are aligned under a unified time reference to form a multi-parameter joint monitoring sequence. Based on the multi-parameter joint monitoring sequence, the correlation analysis of the changes in body temperature, skin resistance and microcirculation velocity over time was carried out to construct a dynamic monitoring sequence that reflects the user's physiological fluctuation rhythm. Real-time trend information of immune activity changes is extracted from dynamic monitoring sequences. The direction of comprehensive changes in body temperature, skin resistance and microcirculation velocity is correlated with the adjustment process of far-infrared radiation output to obtain a continuous data basis for immune activity changes.

3. The graphene wall application management method based on user immune demand profiles according to claim 2, characterized in that, Based on the real-time trend of immune activity obtained from dynamic monitoring sequences, the steps for time-synchronized adjustment of the far-infrared radiation power of the graphene wall surface include: After obtaining the real-time trend of changes in immune activity in the dynamic monitoring sequence, the continuous change information representing the rate of decline in immune status is extracted, and this continuous change information is used as the basis for time adjustment of radiation power. Based on the rate of decline in immune activity, the temporal distribution of far-infrared radiation is synchronously adjusted. When the rate of decline in immune activity increases, the radiation power is gradually reduced, and when the rate of decline in immune activity is stable, a constant radiation output is maintained. Based on the time-synchronized adjustment of far-infrared radiation power, adaptive slowing control is implemented on the energy release process. By gradually adjusting the rate of power change over a continuous period of time, a slowing process of heat release is achieved in the time dimension to prevent local heat accumulation. During the adaptive slowdown of energy release, the rhythm of heat release is continuously controlled, maintaining a moderate energy output during the decline of immune activity and gradually restoring radiation power during the recovery of immune activity.

4. The graphene wall application management method based on user immune demand profiles according to claim 3, characterized in that, In the adaptive slowdown process of energy release, during the step of continuously controlling the heat release rhythm, the radiation output power is gradually adjusted in the time dimension according to the change in the rate of decline of immune activity, and the radiation power is gradually restored in the immune activity recovery phase according to the time synchronization principle.

5. The graphene wall application management method based on user immune demand profiles according to claim 3, characterized in that, During the energy release slowdown process, the steps for continuously rearranging the spatial distribution of local radiation hotspots on the wall surface based on the current far-infrared radiation output state include: During the energy release slowdown process, based on the current far-infrared radiation output state, the radiation energy distribution data of different areas of the wall surface in the time dimension is obtained, and the radiation intensity, temperature change rate and energy output duration of each area are recorded to form thermal response characteristic data. Based on thermal response characteristic data, the heat distribution status of different areas of the wall is identified, the location and heat intensity differences of local radiation hotspots and cooling zones are determined, and a local spatial radiation status distribution map is formed. Based on the principle of time difference compensation, the proportion of radiation intensity in each region is redistributed. By delaying or advancing the duration of radiation output in each region, dynamic coordination of energy release is achieved in the time dimension. Based on the redistribution of radiation intensity ratios in each region, the overall spatial heat distribution is continuously regulated. Spatial stability of energy distribution is maintained through balancing processes, forming a dynamic equilibrium between overheated and cooling zones in both time and space.

6. The graphene wall application management method based on user immune demand profiles according to claim 5, characterized in that, In the process of continuously regulating the overall spatial heat distribution, the heat is kept fluid in space by balancing the rate of change of radiation intensity in different regions. When a certain region shows a trend of heat accumulation, the energy release time of that region is delayed, allowing heat energy to diffuse to adjacent regions. At the same time, the energy gradient change between adjacent regions is controlled on the basis of time synchronization.

7. The graphene wall application management method based on user immune demand profiles according to claim 5, characterized in that, Based on the dynamic equilibrium results of the radiation intensity distribution, the steps for performing periodic corrections on the far-infrared radiation band include: After obtaining the dynamic equilibrium result of the radiation intensity distribution, the current far-infrared radiation output state is periodically identified to determine the energy release cycle and radiation frequency distribution characteristics of different regions, and the radiation cycle of the energy concentration area is time-correlated with the immune activity rhythm. Based on the radiation output characteristics of the energy concentration area, the far-infrared radiation band is mapped to form a time and space distribution map of the radiation band, and the bands that exceed the safe absorption range of the human body are identified and calibrated. Based on the band mapping results, the radiation power in the energy concentration area is periodically corrected. By extending the radiation period or reducing the radiation peak value, the power output is adjusted to form a flexible transition of energy release within the safe band range. Based on the periodic correction of radiation power in the energy concentration area, rhythm matching control is performed on the overall far-infrared radiation band, and the radiation output frequency is dynamically matched according to the periodic characteristics of immune activity changes.

8. The graphene wall application management method based on user immune demand profiles according to claim 7, characterized in that, During the rhythm matching control process, the corrected far-infrared radiation band is continuously adjusted in the time dimension according to the periodic characteristics of immune activity changes. When immune activity is in the declining phase, the radiation power is kept in a mild range. When immune activity is in the recovery phase, the radiation power gradually increases. When immune activity is in the stable phase, the radiation power is maintained at a constant output.

9. The graphene wall application management method based on user immune demand profiles according to claim 7, characterized in that, Based on the periodic correction results of the far-infrared radiation band, the steps for continuously and smoothly controlling the overall radiation output rhythm include: After obtaining the periodic correction results of the far-infrared radiation band, the variation law of the corrected radiation output in the time dimension is collected to determine the initial state of the overall radiation output rhythm and form a basic sequence reflecting the periodic changes in energy release. The collected radiation output rhythm is fused with the immune fluctuation rhythm reflected in the dynamic monitoring sequence to establish a matching relationship between energy release and immune status on the time axis, so that the change in radiation output rhythm and immune fluctuation rhythm form a dynamic correspondence. Based on the integration of immune fluctuation rhythm and radiation output rhythm, the overall radiation output rhythm is continuously and smoothly regulated. By adjusting the energy release time interval and rate of change, the stability and continuity of the heat energy output process are maintained. Based on the correspondence between the fused radiation output rhythm and the immune fluctuation rhythm, the overall thermal environment is gently regulated to maintain a synchronous and stable relationship between the far-infrared radiation output intensity and the immune status.

10. The graphene wall application management method based on user immune demand profiles according to claim 9, characterized in that, In the step of continuously and smoothly regulating the overall radiation output rhythm, the rate of change of radiation power is smoothly transitioned between adjacent time periods by extending the time interval. During the energy release process, the energy release interval is extended when the radiation output rate increases and shortened when the radiation output rate decreases.

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