Evidence map›Paper›PMID 33267159›Full record

ArticleEntropy (Basel, Switzerland)2019

A Novel Signal Separation Method Based on Improved Sparse Non-Negative Matrix Factorization.

Huaqing Wang, Mengyang Wang, Junlin Li, Liuyang Song, Yansong Hao

Abstract read
In one paragraph

Article in Entropy (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Huaqing WangCollege of Mechanical & Electrical Engineering, Beijing University of Chemical Technology, Chao Yang District, Beijing 100029, China.ORCID 0000-0001-5333-0829
Mengyang WangCollege of Mechanical & Electrical Engineering, Beijing University of Chemical Technology, Chao Yang District, Beijing 100029, China.
Junlin LiCollege of Mechanical & Electrical Engineering, Beijing University of Chemical Technology, Chao Yang District, Beijing 100029, China.
Liuyang SongBeijing Key Laboratory of High-end Mechanical Equipment Health Monitoring and Self-Recovery, Beijing University of Chemical Technology, Beijing 100029, China.ORCID 0000-0003-4297-1668
Yansong HaoCollege of Mechanical & Electrical Engineering, Beijing University of Chemical Technology, Chao Yang District, Beijing 100029, China.

Funding

National Natural Science Foundation of China 51675035National Natural Science Foundation of China 51805022
6 · The paper itself

Abstract

In order to separate and extract compound fault features of a vibration signal from a single channel, a novel signal separation method is proposed based on improved sparse non-negative matrix factorization (SNMF). In view of the traditional SNMF failure to perform well in the underdetermined blind source separation, a constraint reference vector is introduced in the SNMF algorithm, which can be generated by the pulse method. The square wave sequences are constructed as the constraint reference vector. The output separated signal is constrained by the vector, and the vector will update according to the feedback of the separated signal. The redundancy of the mixture signal will be reduced during the constantly updating of the vector. The time-frequency distribution is firstly applied to capture the local fault features of the vibration signal. Then the high dimension feature matrix of time-frequency distribution is factorized to select local fault features with the improved SNMF method. Meanwhile, the compound fault features can be separated and extracted automatically by using the sparse property of the improved SNMF method. Finally, envelope analysis is used to identify the feature of the output separated signal and realize compound faults diagnosis. The simulation and test results show that the proposed method can effectively solve the separation of compound faults for rotating machinery, which can reduce the dimension and improve the efficiency of algorithm. It is also confirmed that the feature extraction and separation capability of proposed method is superior to the traditional SNMF algorithm.

Indexed as

compound faults diagnosisSparse non-negative matrix factorizationtime–frequency distributionunderdetermined blind source separation

Identifiers

PMID33267159
PMCPMC7514934

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.