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Adaptive active decoding and novel disjunctive...
Journal article

Adaptive active decoding and novel disjunctive graph-based improved genetic algorithm for multi-type machine robot cell scheduling in mass customization

Abstract

Mass customization represents a critical evolution in modern manufacturing. To achieve efficient large-scale production of low-volume and high-variety products, designing optimized robot cells for flexible automation has become a universal challenge for manufacturers. While our prior research has effectively addressed scheduling problem in robot cells with discrete processing machines (DPMs, each processing one job at a time), the integration of both DPMs and batch processing machines (BPMs, each process multiple jobs simultaneously) introduces significant complexity for fully utilizing productive capacities. This paper investigates the Multi-Type Machine Robot Cell Scheduling Problem (MRCSP) incorporating both DPMs and BPMs and the objective is to minimize makespan. Firstly, a mixed-integer linear programming (MILP) model is formulated to describe MRCSP exactly. Recognizing the challenge of converting batch-aware two-vector encoding into feasible schedules, an adaptive active decoding strategy termed selective insertion batch decoding (SIBD) is proposed. An improved genetic algorithm (IGA) is then developed integrating this tailored encoding/decoding approach and a novel disjunctive graph. Furthermore, a batch neighborhood structure (BN) leveraging problem-specific characteristics is designed. The proposed MILP and IGA were validated on three FJSP-BPM benchmarks. Computational results demonstrate that IGA outperforms existing methods across all instances. In real-world production case studies, the approach achieved a 15.02 % average makespan reduction compared to prior methods, significantly improving resource utilization at a robot cell in southern China.

Authors

Teng Y; Wang T; Li X; Zhang C; Gao L; Wang Z; Shen W

Journal

Robotics and Computer-Integrated Manufacturing, Vol. 100, ,

Publisher

Elsevier

Publication Date

August 1, 2026

DOI

10.1016/j.rcim.2026.103246

ISSN

0736-5845

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