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Venturini had certified that the max voltage transfer ratio of matrix converter is only 0.866 in linear modulation band in theory[1].
These two new topological circuits with similar characteristics: 1.
IEEE Trans. on Power Electronics, Vol. 4, No. 1, January 1989, 4(1): 101-112
[2] J.Holtz,and U.Boelkens, IEEE Transon Industrial electronics, 1989,36(4): 475-479
Proceedings of the IEEE International Symposium on Industrial Electronics, ISIE '96. 1996, 1:466-469

Lemma 1 [55,56].
Table 1.
Chaos. (2013) 1-7
Wang, Generalized finite time synchronization between coupled chaotic systems of different orders with unknown parameters, Nonlinear Dyn. 74 (2013) 479-485
(CISIA 2015), Atlantis Press, 2015, pp. 479-482

Ce(1-x)MXO2, {M=Ru, In} Solid Solutions as Novel Gas Sensors for CO Detection R.
This can be done mainly by three mechanisms, referred to as compensation vacancy (Eq. 1), dopant interstitial compensation (Eq. 2) or interstitial compensation (Eq. 3), according to the following scheme: xMO1.5 + (1-x) CeO2 ↔ xM'Ce + 0.5xVδ + (1-x)CeCe + (2-0.5x)O0, (1) xMO1.5 + (1-x) CeO2 ↔ 0.25xMi*** + 0.75xM'Ce + (1-x)CeCe + (2-0.5x)O0, (2) xMO1.5 + (1-x) CeO2 ↔ xM'Ce + 0.25xCei**** + (1-1.25)CeCe + (2-0.5x)O0, (3) where: O0 and CeCe oxygen and cerium in their respective net sites, Vδ oxygen vacancy, Cei**** cerium ion at interstitial position, (*) effective positive charge, (') effective negative charge.
Figure 1.
References [1] B.
Reddy, J Alloys Comp 479 (2009) 589-593

This new process is schematically shown in Fig.1.
Fig.1 New process for making Ni (and Mn) free stainless steel.
References [1] R.
Forum Vol. 475-479 (2005), p. 2317
[13] Mitsuo Niinomi, Toshikazu Akahori, Tsutomu Takeuchi, and Shigeki Katsura: Materials Science Forum, Vols. 475-479 (2005), p. 2303

The calculation was the equation (1)
It was because that the anoxic zone 2 and aerobic 1 took place in turn, and the experiment was operated under the volume ratio of anaerobic/anoxic/aerobic of 1/0.5/3.6 and 1/1.7/2.4 alternatively.
Reference [1] G.
Water Sci Technol, 1996, 34 (1) : 119 - 128
Water Sci Technol, 2001, 43(1): 155-164

Intrinsic and extrinsic CMR have been recognised as the origin of MR in manganite [1].
There are three stages of weight loss in NSMO precursor powder as illustrated in Fig. 1.
Fig. 1.
Table 1.
References [1] K.

Table 1.
Mix proportions per 1 m3.
Each randomly taken sample weighed approximately 1 kg.
Fig. 1 Average values of compressive strength.
References [1] T.C.

description material 1 1800 01 Long Front Memb 90x90x5 MS 1 844x180 02 Tracker Frame 100x10 MS Sheet main frame sub-assembly Scale 1:5 Projection 3rd Angle FMDU & K.
Components of DLMS: The DLMS consists of ten classes, as shown in Table 1.
Technology Number Allocation: The technology number is allocated as per the following procedure: 1.
In this case, these numbers appear in the bill of materials (BOM) as Part No., (see Figure 1).
Picturing Machines 1400-1700, Cambridge, MIT Press, 2004, pp. 1-10

[1].
The near band gap emission (NBE) occurs at 411-412 nm and the blue or deep level emission (DLE) is at 479-481 nm.
Templating agent D [nm] NBE [nm] DLE [nm] RΩ [kΩ] RCT [kΩ] σ [µS m-1] C [pF] T-80 9 411 479 0.86 64 157 542 PVP-PEG 17 412 481 1.11 67 178 435 Photoelectrical properties.
Comparative dye-degradation profiles [0.020 g-catalyst loading, 7.8 mL s-1 airflow rate, 9.3 mg L-1 dissolved O2, 365 nm, 25.4 μEinstein L-1 s-1, 5.5 pH, 25 mL dye solution].
References [1] X.

Other components include bicyclo[3.1.0]hex-3- en-2-one, 5-(1-methylethyl)- (2.3%), 2-cyclohexen-1-ol,1-methyl-4-(1-methylethyl)-,(1R,4S) (0.9%), bicycle[3.1.1]heptan-3-ol,6,6-dimethyl-2-methylene-,(1S,3R,5S)-(trans-pinoca, 3.7%), 2,6-dimethyl- 2,6-Octadiene (3.9%), 3-thujene (0.3%), palmitic acid (0.2%), stearic acid (0.2%), etc.
(Table 1).
Table 1.
Remaining time (min) Area (%) Compound 1 7.5 0.252 3-Thujene 2 7.7 1.009 (1S)-(-)-alpha-Pinene 3 7.9 1.135 Camphene 4 8.4 1.589 Sabenene 5 8.5 1.387 beta-Pinene 6 9.4 16.494 Benzene,1,2,3,4-tetramethyl- 7 9.5 0.605 Cyclohexene,1-methyl-4-(1-methylethenyl)-, (4R)- 8 10.1 0.202 g-Terpinene 9 10.2 2.648 Cyclohexanol, 1-methyl-4-(1-methylethenyl)-, cis- 10 10.3 0.151 4-Methylphenol 11 10.6 0.101 1-methyl-4-(1-methylethenyl)-Benzene 12 10.9 2.320 Bicyclo[3.1.0]hex-3-en-2-one, 5-(1-methylethyl)- 13 11.2 0.933 2-Cyclohexen-1-ol,1-methyl-4-(1-methylethyl)-, (1R,4S) 14 11.6 3.707 Bicyclo[3.1.1]heptan-3-ol,6,6-dimethyl-2-methylene-, (1S,3R,5S)- 15 12.1 2.976 L(-)-Borneol 16 12.3 4.338 Terpinen-4-ol 17 12.5 4.439 (−)-Myrtenal 18 13.9 0.555 4-(1-methylethyl)-1-Cyclohexene-1-carboxaldehyde 19 14.0 0.504 6-Octen-1-ol,3,7-dimethyl-,1-formate 20 14.3 20.151 L-bornyl acetate 21 15.1 0.378 7-Ethenyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro- 6-hydroxy-1,4a,7-trimethyl-1-phenanthrenecarboxyl 22 15.3 3.884
Lambert: Can J Physiol Pharmacol. vol. 87 (2009), p, 479-492