SYSTEM, MACHINE-READABLE MEDIUM AND METHOD FOR PROCESSING QUALITY DATA OF FORMATION FLUID SAMPLES Russian patent published in 2021 - IPC E21B49/08 G01N1/10 G06F30/20 

FIELD: data processing.

SUBSTANCE: invention relates to the field of data processing, namely the quality data of samples of reservoir oils. A method for processing data on the quality of samples of reservoir oils, performed using at least one processor, includes the following steps: a project is formed to assess the quality of samples, including at least one control sample and at least one target sample and their identifiers; scenarios of criteria are formed, and each scenario includes one or more acts, where: each act is assigned a correspondence to a planning stage or a stage of work, acts are linked in a sequence, after execution, for each act, its coefficient k is formed, the act may be associated with a mandatory transition to the next act or be a terminal act that completes the processing of the scenario, or the act may indicate the possibility of completing the scenario with the formation of the coefficient k, or the act may indicate a possible completion without the formation of the coefficient k with a proposal for corrective measures; give each criterion scenario a rating r, a criterion weight G; specify the sources of data receipt are specified; set handlers for acts where preliminary processing of data coming from specified sources is required; form a work plan for the selection and quality assessment of samples, including a sequence of criteria scenarios and related entities; procedures for the selection and assessment of the quality of samples are sequentially performed, each procedure is associated with the corresponding generated scenario, and the data obtained during the execution of the procedure is transmitted, with the indication of the sample identifier, to the scenario corresponding to the current procedure, according to the generated work plan, according to the formed work plan, moreover, when the script is executed, the sequential execution of acts occurs, and if during the execution of the act there are critical deviations, then the execution of the script ends and the quality indicator of the sample is reset to zero; in the absence of critical deviations, the quality of the samples is determined on the basis of the generated coefficients k obtained during the execution of the acts, the ratings r of the performed criteria scenarios, the weights of the criteria scenarios G; based on the certain quality of the samples, a decision is made to transport the samples to the research laboratory for further analysis; analyze and profiling the performance of criteria scenarios and, in the presence of discrepancies, form recommendations for eliminating deficiencies and modifying sampling procedures.

EFFECT: improving the efficiency of detecting deviations and managing the quality of samples and the reasons for such deviations, increasing the efficiency of sample processing.

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