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首页> 外文期刊>Записки Российского минералогического общества >Диаграммы  состояния  бинарный  систем   H – парафинов  в  связи  с  их  преобразованием  в  природе
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Диаграммы  состояния  бинарный  систем   H – парафинов  в  связи  с  их  преобразованием  в  природе

机译:H - 石蜡的状态图与其在自然中转换有关的二元系统

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Phase relations within mixtures of n-paraffins have such principal significance as toreveal the crystallochemical nature of hydrocarbonminerals. Phase equilibrium diagrams of three binaryparaffin systems C21H44-C23H48 C19H40-C21H44 andC17H36-C19H40 were plotted by results of themo-X-raystudy of phase transitions of these components andtheir mixtures with various molar ratios (by 10-15variants of composition for each system). The thermo-X-ray method application has allowed for the firsttime to take at these diagrams into account fivecondensed phase states of n-paraffins: orthorhombiccrystalline (Orcrysi), low temperature orthorhombicrotator-crystalline (Orrot.i), intermediateorthorhombic rotator-crystalline (Orroi.l+2), hightemperature hexagonal rotator-crystalline (Hrot.2) andliquid (L). Such a result could not be obtained by theusage of only conventional methods of physicalchemistry analysis. Components C17H36 and C19H40 arein the Orrot.l state even at room tempereture. Thepolymor- phic transition Orrot.l→ Hrot.2 is onlyobserved for the homolog C23H48. Because of thesereasons, at the C21H44- C23H48 diagram five single-phase fields are distinguishible pratically for allthe studied compositions (except only one); at theC19H40-C21H44 diasram these fields are typical onlyfor a part of the compositions, and at the C17H36-C19H40 diagram only four phase fields appear but notfor all the compositions. Every one among the detectedstates is characterized by its own form of the thermalmovement of chain moleculae within crystals of n-paraffins as typical representatives of the rotatorsubstance. Individual features of studied diagrams aredetermined by the length and phase state of the rotator homolog-components.
机译:在N-石蜡的混合物中的相位关系具有渗透烃的结晶性质的主要意义。通过这些组分的相转变的Themo-X-射线的结果和各种摩尔比的血管混合物的主题 - X射线的结果绘制了三元酰烷烃Systems的相平衡图C21H44-C23H48C19H36-C21H44和C17H36-C19H40。热X射线法应用已经允许第一次将这些图中携带,以考虑N-链烷烃的缺陷相位状态:正交晶体(orcrysi),低温正晶均匀调节剂 - 结晶(Orrot.i),中间体植物旋转剂 - 结晶(orroi .L + 2),高温六方旋转剂 - 结晶(HROT.2)和氟酸(L)。通过毫无常规的物理化学分析方法无法获得这种结果。组件C17H36和C19H40即使在室温下也是orrot.L状态。 Phicor-phic转换orrot.l→hrot.2对同源物C23H48唯一。由于替代,在C21H44- C23H48图中,五个单相场地可酌情酌情用于所有研究的组合物(仅限除外);在TheC19H40-C21H44 Diasram这些领域才是典型的,只是组合物的一部分,并且在C17H36-C19H40图中仅出现四个相场,但不适合所有的组合物。探测器中的每个人的特征在于其自身形式的链分子的热饲料,其在N-链烷烃的晶体中作为旋转器ubstance的典型代表。由旋转器同源物组件的长度和相位产生的研究图的单个特征。

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