ࡱ>  WYVwdq` bjbjqPqPC::{9&L L L L L L L p [[[8[l\\$]l^"^^^_Vct[ewwww='xIpI$Fh݈9L o__oo݈L L ^^pppoL ^L ^vpowpp: s,L L s^] l(}[oLs s,0\Vs.osL sPfD[hpiLEkKfff݈݈pfff\oooo$$ <<`  hl L L L L L L  A concise and accurate title of study aFirst F. Author, bSecond Author, a,bT. Third Author aInstitution, address bAnother Institution, address Corresponding author: Academic Title, Full Name; e-mail Address; Correspondence Address Received [Dates will be filled in by the Editorial office] The abstract of the manuscript starts here. It is a brief summary (up to 200 words) of the principal, novel results and conclusions obtained. Within this part of the manuscript, abbreviations and numerical data should not be used excessively. It is highly recommended to keep exactly the formatting of all parts of the manuscript, including spacing, margins, fonts, and styles according to this template document. The use of section or page breaks of the word processing software to divide the manuscript into individual chapters or sections should be avoided. The hyphenation of words must not be used either. Keywords: 46 terms characterizing the topic of the manuscript most eloquently Introduction The Introduction contains the formulation of the scientific problem with the references to the results of previous studies dealing with this subject. The reference in the text of the article includes the surname of author(s) and year of publication. The examples to the references given below are as follows: (Stryer, 1988; Cudak & Karcz, 2006; Guiochon et al., 1994) or (J. Hirsch, personal communication). If the names of authors are mentioned in the full sense within the statement, only the year of publication is given in brackets. The above references would then have the forms, e.g. Stryer (1988) has classified ..., Cudak and Karcz (2006) conducted experiments ..., ... was described by Guiochon et al. (1994), or was also obtained by J. Hirsch (unpublished results). If several in-text citations could have the same form, they must be distinguished by letters following the year: for instance Sangeetha et al. (2005a) and (Sangeetha et al., 2005b). While citing multiple references of the same author (group of authors with the same first author) within the manuscript text, reference citation should be abbreviated according to the following examples: (Stryer, 1988; Sangeetha et al., 2004, 2005a, 2005b, 2005c; Amato, 2007) or similar data were published by Stryer (1988) and Sangeetha et al. (2004, 2005a). All cited references should appear in the reference list and vice versa. Theoretical This optional chapter should contain the theoretical analysis of the problem or the description of the computational methods used. All equations, including those describing chemical reactions should be labeled with numerals EMBED Unknown (1) EMBED Unknown (2) Longer sections can be divided into subsections using the styles of the subsection headers as given below. Mathematical modeling Model 1 All mathematical equations should be numbered. The same applies when the equations are referred to in the text. For example, Eqns (3)(5) were used EMBED Unknown (3) EMBED Unknown (4) EMBED Unknown (5) In equations, the symbols of variables must be written in italics. The sub- or superscripts should be written in normal style unless they represent a physical quantity such as pressure in the symbol of cP. The meaning of the symbols should be explained immediately below the equation. All terminology used should comply with the recommendations of the IUPAC  HYPERLINK "http://www.iupac.org/reports/" www.iupac.org/reports/ and  HYPERLINK "http://www.iupac.org/publications/" www.iupac.org/publications/. For the use of quantities, units, and symbols, the following documents are recommended: (  HYPERLINK "http://www.iupac.org/publications/books/gbook/green_book_2ed.pdf" www.iupac.org/publications/books/gbook/green_book_2ed.pdf, (  HYPERLINK "http://www.iupac.org/reports/1993/homann/index.html" www.iupac.org/reports/1993/homann/index.html. A very good overview of the nomenclature in organic chemistry and biochemistry is available at  HYPERLINK "http://www.chem.qmul.ac.uk/iupac/" www.chem.qmul.ac.uk/iupac/. Experimental The experimental chapter should contain basic information about chemicals, experimental and analytical equipment, as well as experimental and mathematical techniques used to obtain the results presented. Detailed information about well-known facts or previously published techniques and illustrative figures, mainly set-up and equipment schemes, should be avoided. Results and discussion This chapter should contain the description of original results presented in the form of tables, schemes, and figures. The original results should be explained and discussed in the text. The tables and figures should be numbered, starting from 1. They should be embedded within the document, approximately in the place, where they should appear in the publication. Figures should be pasted into the Word document so that they could be edited using the software in which they were created. Table 1. Change of reactant concentrations during esterification reaction t/min05103060240cAA*/(mol dm-3)2.011.561.000.650.520.49cP/(mol dm-3)5.004.603.893.603.453.46*Not measured values but obtained from the material balance. cAA concentration of acetic acid, cP concentration of propanol. Tables 13 demonstrate the typical layouts of tables. It is recommended to use the Table tool of Word. Only tabulators, not spaces should be used to align the data. Tables 2 and 3 are the recommended formats of the presentation of extensive characterization data of newly synthesized compounds. Schemes and charts with complex reactions and compounds, respectively, are considered figures and numbered consecutively in order of appearance in the text. Chemicals are denoted by roman numerals according to their order of appearance in the text. For illustration, Fig. 1 represents the reaction of 2H-5-amino-6-cyano-3,7-dioxothiazolo[2,3-b]pyrimidine, I, with trichloroacetonitrile, II, and with phenyl isothiocyanate, III, yielding thiazolo[2,3-b]pyrimido[4,5-d]pyrimidine derivatives IV and V, respectively. The composition and properties of the corresponding products are summarized in Tables 2 and 3.  EMBED ISISServer  Fig. 1. Reactions of 2H-5-amino-6-cyano-3,7-dioxothiazolo[2,3-b]pyrimidine (I). Table 2. Characterization data of newly prepared compounds CompoundFormulaMrwi(calc.)/% wi(found)/%YieldM.p.CHNS%CIVC9H4N5O2SCl3352.5830.65 30.581.14 1.0919.86 19.789.09 9.0181163VC21H14N6O2S2446.5156.48 56.413.16 3.1118.82 18.7614.36 14.2886184 Table 3. Spectral data of newly prepared compounds CompoundSpectral dataIVIR,  EMBED Equation.3 /cm-1: 712 (CCl), 1680 (CO), 3250 (NH2) 1H NMR (DMSO-d6), (: 3.39 (s, 2H, CH2), 5.7 (br, s, 2H, NH2) D2O exchangeable 13C NMR (DMSO-d6), (: 28.3 (CH2), 129.4 (C), 131.1 (C), 164.2 (CO) MS, m/z (Ir/%): 352 (19.8) (M+)IVIR,  EMBED Equation.3 /cm-1: 1170 (C==S), 1600 (C==N), 1655 (Ph), 1676 (CO), 3348 (NH) 1H NMR (DMSO-d6), (: 4.85 (s, 1H, thiazole ring), 7.408.12 (m, l0H, 2Ph) 13C NMR (DMSO-d6), (: 29.3 (CH), 128.5(C), 183.2 (CS) MS, m/z (Ir/%): 446 (56.6) (M+) Figures must be supplied in the true reproduction size, as legible black-and-white vector graphics or bitmaps with the minimum resolution of 900 dpi. Color bitmaps are accepted for the electronic version of the journal but the authors are charged for the color print. It is recommended to optimize the size of the color palette used in order not to increase the file size exorbitantly. At sending the final, revised manuscript, each bitmap figure should also be sent as a separate file in a bitmap format (bmp, gif, tif, jpg, etc.). Ordinary figures should fit the width of the journal column, which is 8 cm. Large figures are allowed to be sized to the whole width or height of the printed area. Fig. 2 illustrates the recommended form of graph and its caption. The symbols of variables must have the same form and style as in the main text. No legend should be included inside the plot area in order to keep the figures legibility. If the plot contains several curves, these can be distinguished by numbers (Fig. 2). The symbols used must be explained in the figure caption. The so-called Type 1 fonts, which include the most frequently employed ones, such as Arial, Helvetica, Times New Roman, should be used for the axis description. The recommended fonts are Arial or Helvetica. Some deviations from this form are allowed, if a unified form of figures is used within the manuscript.  EMBED Excel.Chart.8 \s  Fig. 2. Substrate consumption at 20 C (line 1), 30 C (line 2), and 35 C (line 3). If several plots are included into one figure, they should be distinguished by italicized letters in the left-hand (right-hand, in case of the lack of space) top corner of the plots (Figs. 3a and 3b). It is recommended to use the symbols of variables not their names in the axis titles. The axes values should not have more than three digits. In order to avoid that, the axis quantity should be multiplied by an appropriate factor (Fig. 2). The semi-logarithmic form of axes values should not be used, except for logarithmic axes (Fig. 4).  EMBED Excel.Chart.8 \s  EMBED Excel.Chart.8 \s Fig. 3. Simulated liquid phase compositions (mole fractions of methanol (() and pyridine (()) within the batch distillation column at the beginning, t = 0 h (a), and end of the mixture separation, t = 5 h (b).  EMBED Origin50.Graph  Fig. 4. Variation of the dimensionless mixing time with the modified Reynolds number using pitched blade turbine. Conclusions This optional section contains the principal findings and descriptions of novelty presented in the manuscript. This brief summary is provided for readers who have already read the whole paper. Therefore, it should not be a re-worded abstract. Unlike an abstract, the Conclusions section may include references to figures and tables in the paper itself. Acknowledgements. This is the style in which the acknowledgements should be written. Symbols This optional chapter is useful if numerous symbols are used repeatedly throughout the main text. It should be prepared in the form showed below. All symbols, names, and units of variables used throughout the manuscript must be included in alphabetic order. Bih dimensionless parameter (= aRP/lu) C molar concentration mol m-3 cp specific heat capacity J kg-1 K-1 T temperature K t time h Greek Letters ( heat transfer coefficient W m-2 K-1 (p porosity of particle Subscripts C carbon References This chapter contains cited literature found in the main text arranged in alphabetic order regarding the first authors surname. The form of cited articles, books, presentations at conferences, patents, monographs, etc. should comply with the APA citation style ( HYPERLINK "http://apastyle.apa.org/" http://apastyle.apa.org/). An inseparable part of cited literature is the respective Digital Object Identifier (DOI) number, if available. Amato, I. (2007). Experiments of concern. Well-intentioned research, in the wrong hands, can become dangerous. Chemical & Engineering News, 85(31), 5155. Amazing Amazon region. (1989, January 12). New York Times, p. D11. Bergmann, P. G. (1993). Relativity. In The new Encyclopedae Britannica (Vol. 26, pp. 501-508). Chicago: Encyclopedae Britannica. Cudak, M., & Karcz, J. (2006). Momentum transfer in an agitated vessel with off-centred impellers. Chemical Papers, 60, 375380. DOI: 10.2478/s11696-006-0068-y. Grznrova, G. (2004). Transport phenomena in chromatographic bioseparations. Ph.D. thesis, Slovak University of Technology, Bratislava. Guiochon, G., Shirazi, S. G., & Katti, A. M. (1994). Fundamentals of preparative and nonlinear chromatography. Boston: Academic Press. Hammond, T. (2000, November 20). YAHC: Handle Parameters, DOI Genres, etc. Message posted to Ref-Links electronic mailing list, archived at  HYPERLINK "http://www.doi.org/mail-archive/ref-link/" http://www.doi.org/mail-archive/ref-link/msg00088.html Johnson, A. (2000). Abstract computing machines. Berlin/Heidelberg: Springer. Retrieved March 30, 2006, from  HYPERLINK "http://springerlink.com/content/w25154" http://springerlink.com/content/w25154. DOI: 10.1007/b138965. Liffers, M. (2006, August 30). Finding information in the library. Lecture notes distributed in the unit Functional Anatomy and Sports Performance 1102, University of Western Australia, Crawley, Western Australia. Ludwig, T. (2002). PsychInquiry [computer software]. New York: Worth. Ministerial Council on Drug Strategy. (1997). The national drug strategy: Mapping the future. Canberra: Australian Government Publishing Service. Onderkov, Z., Bryjak, J., VaHkov, K., & Polakovi , M. (2007). Thermal stability of fructosyltransferase. In Proceedings of the 34th International Conference of Slovak Society of Chemical Engineering, May 21 25, 2007 (Po-Tu-4, 116p.pdf, pp. 1 11). Tatransk Matliare: Slovak Society of Chemical Engineering. Osgood, D. W., & Wilson, J. K. (1990). Covariation of adolescent health problems. Lincoln: University of Nebraska. (NTIS No. PB 91-154 377/AS). Poulsen, P. B., & Buchholz, K. (2003). History of enzymology with emphasis on food production. In J. R. Whitacker, A. G. Voragen, & D. W. S. Wong (Eds.), Handbook of food enzymology (pp. 1120). New York: Marcel Dekker. Sangeetha, P. T., Ramesh, M. N., & Prapulla, S. G. (2004). Production of fructo-oligosaccharides by fructosyltransferase from Aspergillus oryzea CFR 202 and Aureobasidium pullulans CFR 77. Process Biochemistry, 39, 755760. DOI: 10.1016/S0032-9592(03)00186-9. Sangeetha, P. T., Ramesh, M. N., & Prapulla, S. G. (2005a). Recent trends in the microbial production, analysis and application of fructooligosaccharides. Trends in Food Science & Technology, 16, 442457. DOI: 10.1016/j.tifs.2005.05.003. Sangeetha, P. T., Ramesh, M. N., & Prapulla, S. G. (2005b). Maximization of fructooligosaccharide production by two stage continuous process and its scale up. Journal of Food Engineering, 68, 5764. DOI: 10.1016/j.jfoodeng.2004.05.022. Sangeetha, P. T., Ramesh, M. N., & Prapulla, S. G. (2005c). Fructooligosaccharide production using fructosyl transferase obtained from recycling culture of Aspergillus oryzae CFR 202. Process Biochemistry, 40, 10851088. DOI: 10.1016/j.procbio.2004.03.009. Smith, I. M. (1988). U.S. Patent No. 123,445. Washington, D.C.: U.S. Patent and Trademark Office. 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M43d" 444e          e          e ~v  <NMM? &] (  @"(<~?<~?3` 1 ?`  @` v A` 1 B` 9J` 9K` 9L?v3d23 M NM4 %%3Q tDQ ; %Q ; %Q3_  NM  MM<4EC3% M*3O& Q444 %%3Q tWQ ;!!%Q ; %Q3_  NM  MM<4EC3% M*3O& Q444 %%3Q QQ ;%Q ; %Q3_  NM  MM<4EC3% M*3O& Q444 %%3Q nDQ ;%Q ; %Q3_  NM  MM<4EC3% M*3O& Q444D$% M 3O&?Q4$% M 3O&BQ4FAp h 3O | 3*w@N@>@#M&!  M43*N@\@4@$@#M&!  M4% 5M3O?&@Q time/min'4% AuMZ3O&AQ  t/C'4523 O NM43d" E3OS@% M,3O& Q423 M NM443_ M NM ] MM<444Ap h 3O3*#M! M43*i@I@9@#M&!  M4% JMZ3O &JP"JK J LJKJQ 6Q/(GJ h-1), nD/(kmol h-1)'43d" 444%e                        !!!!""""####$$$$e                        !!!!""""####$$$$e >@A   :::7 @  dMbP?_*+%"<~?<~?nU} }  9888;8;8;8;88;88 8 8 8 8 88;8;8;8;8;8;8;8;8;8;8;8;8;8;8;8;8;8    &!b 7  7Af@@!ʡ(@6[ ?):/@ %mW\rSm@%}?:%: ? $DDDDDD%%2?- "4AW?DDDD !  2  ,  - . / 0 1 , - . / 0H7  1LJ U@ʡ(@ 6[ ?  "~ %:%$DDDDDD~ %  #"  ! Ւhg@ DD 7Of@D!V~@ D D !Cר? D D !ҋru? DD  ~ p@!\)횩@ D D!4Zh@ DD!? DD!w>? DDH7   -[ A2@6[ ?):/@  "~ %:% $DDDDDD~ %  #"  ! 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M43*???#M&!  M4% 37M3O<&'Q time/min'4% (}0MZ3OX&'Q  mole fraction'4523 O NM43d" M_E3OJZS % M,3O& Q423 M NM443_ M NM ] MM<4444e          e          e ~v  <NMM? p$] B  @"B<~?<~?3` 1 ,`  -` 1 .3d23 M NM4 3Q methanolQ ;Q ; Q3_  NM ] MM<4EC3% M*3O& Q444 3Q pyridineQ ;Q ; Q3_  NM ] MM<4EC3% M*3O& Q444D$% M 3O&,Q4$% M 3O&.Q4FAo ~ 3O^ 3*@o@I@9@#M&!  M43*???#M&!  M4%  ?8M3O<&-Q time/min'4% (1MZ3OX&-Q  mole fraction'4523 O NM43d" j}3OkS#% M,3O& Q423 M NM443_ M NM ] MM<4444e          e          e ~v  <NMM?'9] C  @"C<~?<~?3` 1 2`  3` 1 4?3d23 M NM4 3Q methanolQ ;'7Q ;'7Q3_  NM ] MM<4EC3% M*3O& Q444 3Q pyridineQ ;'7Q ;'7Q3_  NM ] MM<4EC3% M*3O& Q444D$% M 3O&2Q4$% M 3O&4Q4FA x 3O[ 3*0@@?#M&!  M43*???N#M&!  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