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1Author    Heinz-Jörg Kurth, Dieter Bieniek, Friedhelm KörteRequires cookie*
 Title    Hochdruckreaktionen, XIII [1] Synthese von(—)Cannabidiol unter hohen Drucken High Pressure Reactions, XIII [1] Synthesis of (—) Cannabidiol at High Pressure  
 Abstract    Cannabidiol 3 has been synthesized under high pressure conditions (7-8 kbar, 150 °C) from Olivetol 1 and trans-p-Menthadien-(2,8) -ol -(1) 2 with 41% yield. The influence of different solvents on the yield has been studied. 
  Reference    Z. Naturforsch. 36b, 275—276 (1981); eingegangen am 17. November 1980 
  Published    1981 
  Keywords    High Pressure, Cannabidiol, Stereospecific Synthesis 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-0275_n.pdf 
 Identifier    ZNB-1981-36b-0275_n 
 Volume    36 
2Author    A. Heinrich-Schramm, W. E. Price, H.-D LüdemannRequires cookie*
 Abstract    h e In flu e n c e o f D ip o le -D ip o le I n te r a c tio n a n d H y d r o g e n B o n d in g U p o n T r a n s la tio n a l D iffu s iv ity in S im p le F lu id s Self-diffusion coefficients of dimethylether have been measured as a function of temperature (185-458 K) and pressure (up to 200 MPa) by pulse-gradient field spin-echo NMR. Calculated activation volumes (AV*) fall from 15 (10-6 m3/mole) at the highest temperature to 7 (10~6 m3/mole) at the lowest. This trend is in keeping with values for other non-associating liquids. Comparison with self diffusion data for propane and ethanol reveals that the translational diffusivity in dimethylether is influenced by the substance's modest dipole moment (1.3 Debye). The effect is small but measur­ able and becomes more pronounced at lower temperatures. S e lf-D iffu s io n in C o m p re s s e d D im e th y le th e r : 
  Reference    Z. Naturforsch. 50a, 145—148 (1995); received October 5 1994 
  Published    1995 
  Keywords    Dimethylether, Diffusion, High Pressure 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0145.pdf 
 Identifier    ZNA-1995-50a-0145 
 Volume    50 
3Author    M. Sandmann, F. Hamann, A. WürflingerRequires cookie*
 Title    PVT and DTA Measurements on trans-4-w-Hexyl- (4'-CyanophenyI)-Cyclohexane (6PCH) up to 300 MPa  
 Abstract    The phase diagram of trans-4-n-hexyl-(4'-cyanophenyl)-cyclohexane, (6PCH) has been estab-lished by high-pressure differential thermal analysis. Specific volumes are presented for temper-atures between 300 and 370 K up to 300 MPa. The p,V m ,T data have been determined for the nematic, isotropic, and (partly, in the neighbourhood to the melting curve) solid phases. Volume and enthalpy changes along the phase transitions have also been calculated. As previously, the p,Vm,T data were used to calculate the volume entropy for the nematic-isotropic transition. The molar volumes along the clearing line T NI (p) enabled us to calculate the molecular field parameter 7 = ain T NI /3ln V NI , being 4.1. 
  Reference    Z. Naturforsch. 54a, 281—286 (1999); received March 13 1999 
  Published    1999 
  Keywords    6PCH, High Pressure, pVT, Phase Transitions, Thermodynamics 
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 TEI-XML for    default:Reihe_A/54/ZNA-1999-54a-0281.pdf 
 Identifier    ZNA-1999-54a-0281 
 Volume    54 
4Author    Albert Würflinger, M. Massalska-Arodż3, S. Urbanb, W. Weissflogc, S. EmstcRequires cookie*
 Title    Thermodynamic Measurements on the Binary System Bis{[2,2-di(w- hexyloxycarbonyl)ethenyl]phenyl} Biphenyl-4,4'-dicarboxylate and 4-w-Octyloxyphenyl 4-/i-Pentyloxybenzoate at Elevated Pressures  
 Abstract    Thermodynamic measurements have been carried out on the binary system of a swallow-tailed liquid crystal A = bis{[2,2-di(n-hexyloxycarbonyl)ethenyl]phenyl} biphenyl-4,4'-dicarboxylate (4DS6) and B = 4-n-octyloxyphenyl 4-rc-pentyloxybenzoate (5 0 /0 8). A filled smectic A phase is induced in the concentration range 0.11 < xA < 0.75. The maximum of the SmA-N transition temperature (365 K) is observed for xA = 0.33. Dilatometric measurements show that the packing density in the filled phases is increased. High-pressure DTA is employed in order to investigate the coexistence range of the liquid crystalline phases and the slopes of the transition lines. The slopes of the melting curves for the mixtures are significantly smaller than those for the pure components. The slopes for the smectic -nematic -isotropic transitions are considerably larger. The coexistence range for the (smectic + nematic) phases does not seem to be pressure-limited, rather it increases with pressure. 
  Reference    Z. Naturforsch. 56a, 658—662 (2001); received July 18 2001 
  Published    2001 
  Keywords    Phase Transitions, DTA, High Pressure, Swallow-tailed Liquid Crystals 
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 TEI-XML for    default:Reihe_A/56/ZNA-2001-56a-0658.pdf 
 Identifier    ZNA-2001-56a-0658 
 Volume    56 
5Author    J. R., D. B., F. K.Requires cookie*
 Title    High Pressure Reactions, IX 1 Isomerizations at High Pressures  
 Abstract    Cyclooctatetraene dimerises at high pres­ sure (12 Kbar, 20 °C) to the isomers 2 and 3. At 120 °C compound 2 isomerises quanti­ tatively to compound 3. The conversion rate of Hexamethyldewarbenzene to Hexamethyl-benzene at high pressures depends on kind of solvent, whereas the influence of tempera­ ture is small in the range between 2 0 ° and ' 80 °C. 
  Reference    (Z. Naturforsch. 30b, 290 [1975]; eingegangen am 17. Oktober 1974) 
  Published    1975 
  Keywords    High Pressure, Cyclooctatetraene, Dimerisation, Hexamethyldewarbenzene, Isomerization 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0290_n.pdf 
 Identifier    ZNB-1975-30b-0290_n 
 Volume    30 
6Author    Rolf-Rüdiger Krüger, W. Alter, AbrielRequires cookie*
 Title    Über das Hochdruckverhalten von Gips On the Behaviour of Gypsum under High Pressure  
 Abstract    The decom position o f gypsum (dehydration) was studied in the pressure range 7 .5 -6 0 kbar and the temperature range 7 5 -4 0 0 °C using a belt type apparatus. Surprisingly, gypsum is rather stable even at pressures greater than 20 kbar contradicting the results o f a calculation o f the space requirement o f the competing phases (A I I -C a S 0 4 + H-,0; Hemihydrate + H20). Only when rising the temperature, as the most important thermodynamic variable for this reaction, the kinetically controlled decomposition starts. N o acceleration o f the dehydration process under shear stress (simple squeezer device) could be detected due to the limited (not geological) time. 
  Reference    Z. Naturforsch. 45b, 1221—1226 (1990); eingegangen am 27. Februar 1990 
  Published    1990 
  Keywords    Gypsum, Hydrates, High-Pressure, D ecom position 
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 TEI-XML for    default:Reihe_B/45/ZNB-1990-45b-1221.pdf 
 Identifier    ZNB-1990-45b-1221 
 Volume    45 
7Author    H. Einz, Jürgen Beister, K. Arl Syassen, Jürgen KleinRequires cookie*
 Title    Phase Transition of N a3As under Pressure  
 Abstract    We have investigated the high pressure behaviour of N a3As by powder X-ray diffraction. At 3.6 G Pa the material undergoes a reversible phase transition from the N a3As structure (P 6 3/ mmc, a = 487.4(8) pm, c = 851.5(20) pm, Z = 2, at 3.6 G Pa) to the Li3Bi structure type (Fm 3m , a = 683.5(15) pm, Z = 4, at 3.6 GaP). The equation of states is given for the pressure range up to 26 GPa. Results are discussed with respect to structural properties of related A3BV-compounds. 
  Reference    Z. Naturforsch. 45b, 1388—1392 (1990); received M arch 7 1990 
  Published    1990 
  Keywords    High Pressure, Crystal Structure, Phase Transition 
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 TEI-XML for    default:Reihe_B/45/ZNB-1990-45b-1388.pdf 
 Identifier    ZNB-1990-45b-1388 
 Volume    45 
8Author    Oliver Schilke, EberhardH. Ohaus, H. Arro Lentz, JeongR. KimRequires cookie*
 Title    HPTLC-Analyse von Ginsenosiden zur Bewertung von Ginseng-Extraktionen mit Methanol-Wasser, Wasser oder Ammoniak HPTLC Analyses o f Ginsenosides for the Evaluation of Ginseng Extractions with M ethanol-W ater, W ater or Am m onia  
 Abstract    Korean Ginseng roots were extracted with m ethanol-w ater, water and liquid and supercriti­ cal ammonia. The yields of the extracts by different methods are reported. The extracts were analyzed by high-performance thin-layer chrom atography. Retention value factors of ginsen­ osides are tabellized. The absolute yields have been measured in mg ginsenoside per g ginseng root for the used standard ginsenosides. Formally the am m onia extraction at 334 K and 26 bar is found to be favourable. The supercritical condition of 418 K and 130 bar leads to a decom­ position of the ginsenosides. Possibilities of fractionation by different solvents or different temperatures are indicated, but attem pts are still required to get fractions o f several extraction agents. 
  Reference    Z. Naturforsch. 46b, 829—834 (1991); eingegangen am 17. Dezember 1990 
  Published    1991 
  Keywords    Ginsenoside, Extraction, H PTLC Analysis, High Pressure 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-0829.pdf 
 Identifier    ZNB-1991-46b-0829 
 Volume    46 
9Author    S. U. Rban, T. Briickert, A. W. ÜrflingerRequires cookie*
 Title    Dielectric Studies on Liquid Crystals under High Pressure: VI. Low Frequency Relaxation Process in the Nematic and Smectic A Phase of 4-n-Octyl-4'-Cyanobiphenyl (8 CB)  
 Abstract    Dielectric relaxation studies of 4-n-octyl-4'-cyanobiphenyl (8 CB) were performed in the pressure range 0 .1 -1 2 0 M Pa, the frequency range 1 k H z -1 3 M Hz and the temperature range 2 9 5-331 K. The dielectric behaviour of 8C B in the nematic phase is similar to that of 5CB, 6C B and 7CB. In particular, the activation enthalpy decreases with increasing pressure and the activation volume decreases with increasing temperature in the nematic phase. In the smectic A phase of 8CB both these parameters are markedly lower and show opposite pressure and temperature dependencies. We tentatively interpret these effects as a result of breaking of the dipole-dipole correlations which manifests itself differently in these liquid crystalline phases. 
  Reference    Z. Naturforsch. 49a, 552 (1994); received March 5 1994 
  Published    1994 
  Keywords    Dielectric relaxation, High pressure, Liquid crystals, Activation quantities 
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 TEI-XML for    default:Reihe_A/49/ZNA-1994-49a-0552.pdf 
 Identifier    ZNA-1994-49a-0552 
 Volume    49 
10Author    Heinrich-Schramm, W. E. Price, H.-D LüdemannRequires cookie*
 Abstract    Self-diffusion in ethanol/hexane and dimethylether/hexane mixtures of various compositions has been measured at 215-350 K and up to 200 MPa. Qualitative analysis of the results indicates that, as expected, hydrogen bonding retards the self-diffusion of ethanol in the mixture, especially at the low temperatures. Dimethylether shows a slight effect of dipole-dipole interactions on the self-diffu­ sion, as seen by a higher AE* value than for the alkane. However there is no significant difference in the pressure dependence for both mixtures. This is shown by considering the ratio of the two diffusion coefficients, which suggests that, contrary to what is observed for pure alcohols, pressure has little effect upon the hydrogen bonding of ethanol in the mixture. In additon, there is surprisingly little concentration dependence on the ratios for either mixture. 
  Reference    Z. Naturforsch. 50a, 149—154 (1995); received October 5 1994 
  Published    1995 
  Keywords    Binary mixtures, Self diffusion, High pressure 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0149.pdf 
 Identifier    ZNA-1995-50a-0149 
 Volume    50 
11Author    Z. NaturforschRequires cookie*
 Abstract    The pressure-dependence of the dielectric anisotropy, Ae = e0||— e0±, of two nematogens, n-pentyl-and n-hexyl-cyanobiphenyl (5CB and 6CB) has been measured at constant temperature. For this purpose a high pressure chamber made of non-magnetic materials was constructed, allowing for the orientation of the samples by a magnetic field. The pressure dependencies of Aex were analyzed in the frame of the Maier-Meier equations for the principal permittivity components in the nematic phase. It was found that the relation between Ae and the order parameter S is not properly described by these equations. The Kirkwood correlation factor calculated on the basis of the present results and the Maier-Meier equations is smaller than 0.5, whereas it increases to a more realistic value (~0.7) if the electronic polarization is incorporated in the equations. P r e s s u r e D e p e n d e n c e o f th e D ie le c tric A n is o tr o p y o f 5 C B a n d 6 C B 
  Reference    Z. Naturforsch. 50a, 826—830 (1995); received April 28 1995 
  Published    1995 
  Keywords    Nematic liquid crystals, Cyanobiphenyls, High pressure, Dielectric anisotropy 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0826.pdf 
 Identifier    ZNA-1995-50a-0826 
 Volume    50 
12Author    A. WiirflingerRequires cookie*
 Title    Nematic Potential and Order Parameter Determined from Dielectric Measurements  
 Abstract    The Maier-Saupe theory is employed in order to calculate order parameters S from the nematic po-tential q. It is found that one of the basic assumptions of the Maier-Saupe theory, q ~S, is approximate-ly fulfilled. The relation between q and S is analysed for various state changes. Previously reported find-ings for 7 PCH that q ~S, not fulfilled along isochoric changes, can be explained by taking into account the pressure and temperature dependences of q. The procedure described in this paper allows to treat experimental data for the nematic potential in a unique way, without being affected by inadequacies of experimentally determined order parameters. 
  Reference    Z. Naturforsch. 53a, 141—144 (1998); received February 11 1998 
  Published    1998 
  Keywords    Liquid Crystals, High Pressure, Nematic Potential, Dielectric Relaxation 
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 TEI-XML for    default:Reihe_A/53/ZNA-1998-53a-0141.pdf 
 Identifier    ZNA-1998-53a-0141 
 Volume    53 
13Author    M. Sandmann, A. WürflingerRequires cookie*
 Title    PVT Measurements on 4'-w-Hexyl-Biphenyl-4-Carbonitrile (6CB) and 4 -w-Heptyl-Biphenyl-4-Carbonitrile (7CB) up to 300 MPa  
 Abstract    P, V m , 7" data were established for 4'-n-hexyl-biphenyl-4-carbonitrile (6CB) and 4'-n-heptyl-biphen-yl-4-carbonitrile (7CB) between 300 and 370 K up to 300 MPa, and specific volumes were determined for the liquid crystalline, isotropic, and also partly for the crystal phases. Volume and enthalpy chang-es at the phase transitions are also presented. In the case of 6CB, a new crystal phase has been detect-ed, corresponding to a triple point at 338 K and 196 MPa. The p, V m , T data enabled us to separate the entropy change into a volume-dependent part and configurational part. From the molar volumes along the nematic-isotropic phase transition T Nl (p), the molecular field parameter y= 3lnT NI /3ln V NI was deter-mined. 
  Reference    Z. Naturforsch. 53a, 233—238 (1998); received March 11 1998 
  Published    1998 
  Keywords    6CB, 7CB, High Pressure, pVT, Phase transitions, Thermodynamics 
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 TEI-XML for    default:Reihe_A/53/ZNA-1998-53a-0233.pdf 
 Identifier    ZNA-1998-53a-0233 
 Volume    53 
14Author    M. Sandmann, A. WürflingerRequires cookie*
 Title    PVT Measurements on 4'-/i-Octyl-Biphenyl-4-Carbonitrile (8CB) up to 300 MPa  
 Abstract    P, V m , Tdata have been measured for the smectic, nematic and isotropic phases of 4'-n-octyl-biphen-yl-4-carbonitrile (8CB) in the temperature range 300-370 K and pressures up to 300 MPa. At atmos-pheric pressure all phase transitions appear to be of first order due to a discontinuity in the density. The volume change at the smectic A -nematic transition is only a tenth of the volume change at the clear-ing temperature. At moderate pressures below 80 MPa the S A -N transition could be detected as a dis-continuity in the period of oscillation in measurements with a high-pressure vibrating tube densimeter. At higher pressures the discontinuity seems to die away, possibly indicating a change from first order to second order transition. From the volume changes and the slopes of the transition lines we calculate the enthalpy changes at the phase transition. The p, V m , T data enable us to calculate the volume part of the entropy and the molecular field parameter y=9ln 7 N i/3ln V NI . 
  Reference    Z. Naturforsch. 53a, 787—792 (1998); received July 10 1998 
  Published    1998 
  Keywords    8CB, High Pressure, pVT, Phase Transitions, Thermodynamics 
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 TEI-XML for    default:Reihe_A/53/ZNA-1998-53a-0787.pdf 
 Identifier    ZNA-1998-53a-0787 
 Volume    53 
15Author    Stanislaw Urban, Albert WürflingerRequires cookie*
 Title    High Pressure Dielectric Studies of a Substance with the Smectic A 1 Phase  
 Abstract    The results of dielectric studies of 5-n-hexyl-2-(4'-isothiocyanato)-l,3-dioxane (6DBT) in the smec-tic A, phase at pressures up to 150 MPa and temperatures up to 340 K are presented. The low frequen-cy relaxation time T\\ (/?, T) yields the activation volume A # V|| = RT(d ln Tjj/9/>) r and activation enthal-py A # //jj = R(d ln T||/37) p . The calculated values of these parameters are compared with those ob-tained recently for n-octyl-cyanobiphenyl (8CB) forming the smectic A d phase. In the case of 6DBT both these quantities are practically constant, whereas those for 8CB decrease, when going away from the phase transitions isotropic -smectic A] (6DBT) or nematic -smectic A d (8CB). These differences support our earlier conclusion that increase of pressure leads to a breaking of the antiparallel associa-tions of cyanobiphenyl molecules in the smectic as well as in the nematic phases. 
  Reference    Z. Naturforsch. 54a, 455—458 (1999); received July 12 1999 
  Published    1999 
  Keywords    Liquid Crystal; Smectic A, Dielectric Properties, High Pressure 
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 TEI-XML for    default:Reihe_A/54/ZNA-1999-54a-0455.pdf 
 Identifier    ZNA-1999-54a-0455 
 Volume    54 
16Author    M. Massalska-Arodź, A. Würflinger, D. BüsingRequires cookie*
 Title    High-pressure DTA Studies of the Phase Behaviors of 4-n -butyl-thiocyanobiphenyl (4TCB) and 4-w-pentyl-4'-n-phenyl-cyanocyclohexane (5HCP)  
 Abstract    DTA measurements of 4-/i-butyl-thiocyanobiphenyl (4TCB) and/?-cyano-/?'-pentylphenyl-cyclohex-ane (5HCP) have been performed in the temperature range 220 K-390 K and pressures up to 400 MPa. For 4TCP a transition from a crystalline to a liquid crystal phase (probably smectic E) could be detect-ed at higher pressures > 90 MPa. The pressure dependence of the transition temperature has been estab-lished. At pressures lower than 88.7 MPa no transition of SmE into a crystal or into a glass has been found. For 5HCP only the melting curve was observed, in contrast to 5PCH, which displays a liquid crystalline nematic phase. 
  Reference    Z. Naturforsch. 54a, 675—678 (1999); received November 5 1999 
  Published    1999 
  Keywords    DTA, High Pressures, Phase Transitions, Liquid Crystals 
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 TEI-XML for    default:Reihe_A/54/ZNA-1999-54a-0675.pdf 
 Identifier    ZNA-1999-54a-0675 
 Volume    54 
17Author    H. Hauer, H.-D Lüdemann, R. JaenickeRequires cookie*
 Title    Free Activation Energies and Activation Volumes for the Amide Rotation in Some Peptides Studied by High Pressure 'H-High Resolution NMR  
 Abstract    From the pressure dependence o f !H high resolution N M R spectra o f two dipeptides (glycylsarcosine and N-acetyl-L-proline-NH-methylamide in the range 0.1 MPa <.p< . 150 MPa the activation volumes A V* for the am ide rotation are derived. This conform ational transition is characterized for glycylsarcosine by A V* = 4 ± 1 cm3 • m ol-1 and for. the proline derivative by AV* = 1 .5 ± 1 cm3 • m ol-1. From the given results the m axim um contribution o f proline cis ^ trans isomerisation to the pressure dependence o f the rate o f reactivation of proteins can be estimated to ~ — 30% per M Pa and proline present. 
  Reference    Z. Naturforsch. 37c, 51—56 (1982); received Septem ber 221981 
  Published    1982 
  Keywords    Activation Volume, High Pressure, NM R, Peptides, Proline-Isom erization 
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 TEI-XML for    default:Reihe_C/37/ZNC-1982-37c-0051.pdf 
 Identifier    ZNC-1982-37c-0051 
 Volume    37 
18Author    SeymourSteven Brody, Karel HeremansRequires cookie*
 Title    Pressure Induced Shifts in Spectral Properties of Pigment-Protein Complexes and Photosynthetic Organisms  
 Abstract    Application o f elevated pressure (up to 1200 bars) results in a bathochrom ic shift o f the absorption bands o f photosynthetic pigments. The photosynthetic system s studied include: photosystem I particles, chloroplasts, acetone extracts o f chloroplasts, A U T particles and light harvesting particles o f Rh. sphaeroides, light harvesting particles o f R26. Sim ilar spectral changes are observed in all systems. The spectral shifts appear to be associated w ith pressure-induced changes in the local electric fields o f the pigm ents, rather than changes in the index o f refraction o f the solvent. 
  Reference    Z. Naturforsch. 39c, 1104 (1984); received June 18 1984 
  Published    1984 
  Keywords    Photosynthesis, Chlorophyll, High Pressure, Reaction Centers, C hlorophyll-Protein C om plexes 
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 TEI-XML for    default:Reihe_C/39/ZNC-1984-39c-1104.pdf 
 Identifier    ZNC-1984-39c-1104 
 Volume    39 
19Author    H. G. Kreul, R. Waldinger, A. WürflingerRequires cookie*
 Title    Differential Thermal Analysis and Dielectric Studies on Neopentanol under Pressure  
 Abstract    Differential thermal analysis (DTA) and dielectric measurements have been performed on 2,2-di-methyl-l-propanol (neopentanol) up to 200 MPa. Neopentanol exhibits at least one orientationally disordered (ODIC) phase (solid I) that transforms at lower temperatures to a non-plastic phase (solid II). There is evidence of a further ODIC phase denoted as solid I'. The pressure dependence of the phase transitions and the dielectric behaviour up to frequencies of 13 MHz are described. Activation enthalpies and volumes are derived from the dielectric relaxation time and compared with results for other alcohols. 
  Reference    Z. Naturforsch. 47a, 1127—1134 (1992); received July 27 1992 
  Published    1992 
  Keywords    High pressure, DTA, Phase transitions, Dielectric constant, and relaxation 
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 TEI-XML for    default:Reihe_A/47/ZNA-1992-47a-1127.pdf 
 Identifier    ZNA-1992-47a-1127 
 Volume    47 
20Author    J. Reuter, T. Brückert, A. WürflingerRequires cookie*
 Title    Differential Thermal Analysis under Pressure on Cyanocyclohexane, 1,2,3,4-Tetrahydro-5,6-dimethyl-1,4-methanonaphthalene, and 2-Methyl-2-propanol  
 Abstract    Differential thermal analysis has been performed on cyanocyclohexane (CCH), 1,2,3,4-tetrahydro-5,6-dimethyl-1,4-methanonaphthalene (TDMN), and 2-methyl-2-propanol (t-butanol) up to 300 MPa. The latter compound was also investigated dielectrically. CCH displays an ODIC phase that transforms only reluctantly to the low-temperature stable phase II. Annealing under pressure can appreciably accelerate this transformation. For all three compounds the phase diagrams were established. For CCH and TDMN also the pressure dependence of the glass transition has been determined. 
  Reference    Z. Naturforsch. 48a, 705—708 (1993); received March 10 1993 
  Published    1993 
  Keywords    High pressure, DTA, Phase transitions, Glass transition, Dielectric constant 
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 TEI-XML for    default:Reihe_A/48/ZNA-1993-48a-0705.pdf 
 Identifier    ZNA-1993-48a-0705 
 Volume    48