Synthesis of Quantum Circuits for Linear Nearest Neighbor Architectures

While a couple of impressive quantum technologies have been proposed, they have several intrinsic limitations which must be considered by circuit designers to produce realizable circuits. Limited interaction distance between gate qubits is one of the most common limitations. In this paper, we suggest extensions of the existing synthesis flow aimed to realize circuits for quantum architectures with linear nearest neighbor (LNN) interaction. To this end, a template matching optimization, an exact synthesis approach, and two reordering strategies are introduced. The proposed methods are combined as an integrated synthesis flow. Experiments show that by using the suggested flow, quantum cost can be improved by more than 50% on average.Comment: 14 pages, 11 figures, 3 table

Lubricant pyrolysis during sintering of powder metallurgy compacts

The chemistry surrounding the pyrolysis of N,N′-ethylenebisstearimide (EBS) compacted with iron powder is described for the first time. Heat treatment is carried out in a 5 vol pct hydrogen atmosphere (balance nitrogen) over the 100 °C to 850 °C range. The exhaust from the furnace is monitored by Fourier transform infrared and dispersive ultraviolet absorption spectroscopy; condensable materials are analyzed by gas chromatography/mass spectrometry (GC/MS). A wide range of analytes emitted from the preceding process were characterized. The aliphatic CH stretch in the 3000 to 2700 cm⁻¹ range and the asymmetric CO stretch in gaseous CO₂ at 2350 cm⁻¹ are excellent indicators of the extent of delubrication. A bimodal CO emission phase is observed in the temperature window between delubrication and sintering. Three major large molecule reaction products, along with five minor compounds, are identified by GC/MS. A preliminary reaction mechanism is inferred based on product analysis and known organic chemistry. It appears that hydrolysis of EBS competes with γ-H abstraction yielding an N-vinyl amide and stearamide, which undergoes further reaction. Hydrolysis affords stearic acid, which decarboxylates to heptadecane, and 2-heptadecyl-4,5-dihydroimidazole via ring closure of the corresponding amino-amide