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Inoue 1,a , K.
Tanaka 1,b , H.
Adachi 1,c, K.
Figure 1.
Forum, 475-479(2005), 619

Table 1 Defining features of the geological structure of the Jurassic deposits.
Fig. 1 Map of the current status of development and interventions done of the YUK11 formation experimental site of the Talinsk area of the Krasnoleninsk field (as of April 1, 2007).
The duration of the technological effect has exceeded 1 year since the completion of the work (Fig. 6).
[m3/day] Specific injectivity [m3/day·atm] Specific injectivity decrease [%] max min aver initial final initial final max min aver max min aver Talinsk, YUK11 MPDC 8 411.8 25.2 186.0 493 410 459 493 338 442 18.8 4.1 78.2 Talinsk, YUK11 DSFC 9 298.9 85.6 218.2 540 345 450 480 320 398 17.5 4.7 73.1 Ershovoye, YUV1 MPDC 3 32.4 25.8 25.9 508 432 457 508 360 423 5.9 3.8 35.6 Vostochno-Surgutskoye, YUS1 DSFC 5 52.9 4.7 34.8 720 350 496 720 332 479 9.3 4.4 52.7 Vostochno-Surgutskoye, YUS 1 DSFC 5 52.9 2.95 23.0 720 350 496 720 332 479 9.3 4.4 52.7 Kinyaminskoye, YUS 11 DSFC 5 93.3 31.6 54.8 480 320 380 467 270 350 2.5 2.2 10.8 Summary and Conclusions The obtained results show that in consequence of the MPDC and DSFC chemical compositions injection, a significant decrease in the specific injectivity of injection wells occurred.
References [1] T.A.

The result showed that alumina-pillared montmorillonite with 1.83nm of basal spacing exhibited a high catalytic activity for the isomerization of α-pinene, and 97.4% conversion of α-pinene was achievedat 373K for 3hwhen the mass ratio of catalyst to α-pinene was 1/10.
Fig.1 XRD patterns of alumina-pillared montmorillonite and Na-montmorillonite According to Fig.1, the basal spacing of d001 reflection is shifted from 1.28nm of the Na-montmorillonite to 1.83nm of the Al-PILM, which confirms the successful modification of Na-montmorillonite by pillaring.
Conclusions (1) Alumina-pillared montmorillonitewith an expansion of the interlayer distances of 1.83nmwas prepared by intercalation with aluminiumpolyhydroxocation as a precursor into Na-MMT layer space of 1.28nm
References [1] Breen C,Moronta A J.Clay Minerals2001,36:467-472
[6] Breen C,WatsonR.Applied Clay Science 1998,12:479-494

The compositions of Al6061 alloys are shown in Table 1.
This was followed by polishing with 6 μm, 3 μm and 1 μm diamond paste.
References [1] H.C.
Basheer, Effect of fly ash addition on the physical and mechanical properties of AA6063 alloy reinforcement, Metals. 7 (2017) 477-479
Sornakumar, Development and properties of aluminium silicon alloy fly ash composites, Powder Metall. 54 (2010) 474–479

De Gendt1,2, 1 1 1 IMEC Interuniversity Microelectronics Center, Kapeldreef 75, B-3001 Leuven, Belgium 2 Katholieke Universiteit Leuven, Celestijnenlaan 200F B-3001, Leuven, Belgium avandorpd@imec.be Keywords: InAs, etching, reoxidation, cleaning, III-V channel, fin-FET Introduction At present, the performance enhancement for Si-based transistors can no longer be guaranteed due to intrinsic mobility issues.
The etch rate is targeted in the <0.1-10 nm min-1 range [3].
The etch rate decreases further when the HCl concentration is increased to 1 M.
In Figure 1(b) the etch rate versus HCl concentration is shown.
References [1] J.A. del Alamo: Nature 479 (2011), p. 317 [2] K.A.

Effect of Mn doping on the photocatalytic photodegradation properties of Zn1−xMnxO nanomaterials Chuanling Men 1, a, Hongqin Li 1,b and Hua Zhang 1,c 1School of energy and power engineering, University of Shanghai for Science and Technology, Shanghai 200093, China a anziloveling@yahoo.com.cn, b tianxinyu0301@163.com, c zhanghua3000@163.com Keywords: Zn1−xMnxO, sol-gel, Photocatalytic photodegradation.
Fig.1 photodecolorization of methyl orange using Zn0.82Mn0.18O as photocatalyst under UV irradiation and under solar light Results and Discussion Methyl orange was solved in water and diluted to a concentration of 3mg/L for the photocatalytic activity study.
Figure 1 illustrates the results of photodecolorization of methyl orange using Zn0.82Mn0.18O as photocatalyst under UV irradiation and under solar light.
Acknowledgement This work is supported by Innovation Program of Shanghai Municipal Education Commission (No. 09YZ219) and Doctoral Fund of Ministry of Education of China (No. 200802520006) and Shanghai Leading Academic Discipline Project (S30503) References [1] R.W.
Ouyang, Journal of Alloys and Compounds 479 (2009) p.

(1), where, v is Poisson ratio; E represents elastic modulus; indicates internal friction angle.
References [1] I.C.Cormeau, O.C.Zienkiewicz.
Eng, 9(1) (1975)109-127
Zhang, Super Gravity Dam Generalized Damage Study, Advanced Materials Research. 479-481 (2012) 421-435 [3] Y.
Ren, Fuzzy Stochastic Generalized Reliability Studies on Embankment Systems Based on First-order Approximation Theorem, Water Science and Engineering. 1(4) (2008) 36-46 [5] Y.

The amount of additives added was 1.5wt%CeO2, 1.5wt%Cr2O3 and the mixture of 1.5wt%CeO2 and 1.5 wt%Cr2O3.
Thermal etching was performed on the polished specimens at a temperature 100oC below sintering temperature for 1 h.
Table 1 Batch composition and sample codes for different batch No.
References [1] A.
Euro.Cer.Soc. 23(2003) 469-479

Fig. 1 Schematic diagram of graft copolymerization Results and Discussions The synthesis design of graft copolymers with different AA and AMPSis listed in Table 1.
H2O/g / ºC Initiator monomers (NH4)2S2O8/g NaHSO3/g ratio AA/g AMPS/g ratio 1 80 75 8 2.7 3:1 20 10 2:1 2 80 75 8 8 1:1 20 10 2:1 3 80 75 8 8 1:1 30 10 3:1 Many factors affect the polymerization process and properties of the final polymer AA-AMPS, such as the monomer mass ratio, reaction concentration, initiator dosage, pH, chain transfer agent, reaction time, stirring speed, the method of monomer addition and reaction temperature.
In this study, the temperature is 75ºC, and the ratio of (NH4)2S2O8/ NaHSO3 is 3:1, the ratio of AA to AMPS is 2:1 and 3:1, the content of monomers and initiator is 34wt%.
Reference [1] F.
Preparation and analysis of a polyacrylate grinding aid for grinding calcium carbonate in an ultrafine wet grinding process [J].Powder Technology, 2014(254),470-479.

Durgadsimi 1, a, S.
Results and discussion XRD patterns of the composites and ferrite Fig. 1 showed well defined peaks.
Fig. 1.
References [1] W.
Comp., 479(2009) 807 [7] E.