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电解质浓度对胶体和晶体某些物理性质的影响。

INFLUENCE OF THE CONCENTRATION OF ELECTROLYTES ON SOME PHYSICAL PROPERTIES OF COLLOIDS AND OF CRYSTALLOIDS.

机构信息

Laboratories of The Rockefeller Institute for Medical Research.

出版信息

J Gen Physiol. 1920 Jan 20;2(3):273-96. doi: 10.1085/jgp.2.3.273.

Abstract
  1. When a 1 per cent solution of a metal gelatinate, e.g. Na gelatinate, of pH = 8.4 is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain rate which can be measured by the rise of the level of the liquid in a manometer. When to such a solution alkali or neutral salt is added the initial rate with which water will diffuse into the solution is diminished and the more so the more alkali or salt is added. This depressing effect of the addition of alkali and neutral salt is greater when the cation of the electrolyte added is bivalent than when it is monovalent. This seems to indicate that the depressing effect is due to the cation of the electrolyte added. 2. When a neutral M/256 solution of a salt with monovalent cation (e.g. Na(2)SO(4) or K(4)Fe(CN)(6), etc.) is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain initial rate. When to such a solution alkali or neutral salt is added, the initial rate with which water will diffuse into the solution is diminished and the more so the more alkali or salt is added. The depressing effect of the addition of alkali or neutral salt is greater when the cation of the electrolyte added is bivalent than when it is monovalent. This seems to indicate that the depressing effect is due to the cation of the electrolyte added. The membranes used in these experiments were not treated with gelatin. 3. It can be shown that water diffuses through the collodion membrane in the form of positively charged particles under the conditions mentioned in (1) and (2). In the case of diffusion of water into a neutral solution of a salt with monovalent or bivalent cation the effect of the addition of electrolyte on the rate of diffusion can be explained on the basis of the influence of the ions on the electrification and the rate of diffusion of electrified particles of water. Since the influence of the addition of electrolyte seems to be the same in the case of solutions of metal gelatinate, the question arises whether this influence of the addition of electrolyte cannot also be explained in the same way, and, if this be true, the further question can be raised whether this depressing effect necessarily depends upon the colloidal character of the gelatin solution, or whether we are not dealing in both cases with the same property of matter; namely, the influence of ions on the electrification and rate of diffusion of water through a membrane. 4. It can be shown that the curve representing the influence of the concentration of electrolyte on the initial rate of diffusion of water from solvent into the solution through the membrane is similar to the curve representing the permanent osmotic pressure of the gelatin solution. The question which has been raised in (3) should then apply also to the influence of the concentration of ions upon the osmotic pressure and perhaps other physical properties of gelatin which depend in a similar way upon the concentration of electrolyte added; e.g., swelling. 5. When a 1 per cent solution of a gelatin-acid salt, e.g. gelatin chloride, of pH 3.4 is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain rate. When to such a solution acid or neutral salt is added-taking care in the latter case that the pH is not altered-the initial rate with which water will diffuse into the solution is diminished and the more so the more acid or salt is added. Water diffuses into a gelatin chloride solution through a collodion membrane in the form of negatively charged particles. 6. When we replace the gelatin-acid salt by a crystalloidal salt, which causes the water to diffuse through the collodion membrane in the form of negatively charged particles, e.g. M/512 Al(2)Cl(6), we find that the addition of acid or of neutral salt will diminish the initial rate with which water diffuses into the M/512 solution of Al(2)Cl(6), in a similar way as it does in the case of a solution of a gelatin-acid salt.
摘要
  1. 当 1%的金属明胶凝胶,例如 pH=8.4 的 Na 凝胶,通过硝酸纤维素膜与蒸馏水分离时,水会以一定的速率扩散到溶液中,这个速率可以通过测量气压计中液体的上升来确定。当向这种溶液中加入碱或中性盐时,水扩散到溶液中的初始速率会降低,添加的碱或盐越多,降低的幅度就越大。当添加的电解质阳离子是二价时,这种添加的抑制作用比单价阳离子时更大。这似乎表明,抑制作用是由于添加的电解质阳离子造成的。

  2. 当中性 M/256 盐(例如 Na(2)SO(4)或 K(4)Fe(CN)(6)等)的溶液与蒸馏水通过硝酸纤维素膜分离时,水会以一定的初始速率扩散到溶液中。当向这种溶液中加入碱或中性盐时,水扩散到溶液中的初始速率会降低,添加的碱或盐越多,降低的幅度就越大。当添加的电解质阳离子是二价时,这种添加的抑制作用比单价阳离子时更大。这似乎表明,抑制作用是由于添加的电解质阳离子造成的。这些实验中使用的膜未经明胶处理。

  3. 可以证明,在(1)和(2)中所述的条件下,水以带正电荷的粒子的形式通过硝酸纤维素膜扩散。在向中性一价或二价阳离子盐溶液中扩散水的情况下,可以根据离子对水的带电和扩散速率的影响来解释添加电解质对扩散速率的影响。由于添加电解质的影响在金属明胶溶液中似乎是相同的,因此就会产生这样一个问题:这种添加电解质的影响是否也可以用同样的方式来解释,如果是这样的话,那么就会进一步提出这样一个问题:这种抑制作用是否必然取决于明胶溶液的胶体性质,或者我们是否不是在处理两种情况下物质的相同性质;即,离子对水通过膜的带电和扩散速率的影响。

  4. 可以证明,代表电解质浓度对水从溶剂扩散到膜另一侧溶液初始速率影响的曲线与代表明胶溶液的永久渗透压的曲线相似。因此,(3)中提出的问题也适用于离子对明胶溶液渗透压和其他可能依赖于添加的电解质浓度的物理性质的影响;例如,溶胀。

  5. 当 pH 为 3.4 的 1%明胶-酸盐溶液,例如明胶盐酸盐,与蒸馏水通过硝酸纤维素膜分离时,水会以一定的速率扩散到溶液中。当向这种溶液中加入酸或中性盐时(在后者的情况下要注意 pH 不发生变化),水扩散到溶液中的初始速率会降低,添加的酸或盐越多,降低的幅度就越大。水通过硝酸纤维素膜以带负电荷的粒子的形式扩散到明胶盐酸盐溶液中。

  6. 当我们用结晶盐代替明胶-酸盐,使水以带负电荷的粒子的形式通过硝酸纤维素膜扩散,例如 M/512 Al(2)Cl(6)时,我们发现,添加酸或中性盐会降低水扩散到 M/512 Al(2)Cl(6)溶液中的初始速率,这种情况与明胶-酸盐溶液中的情况相似。

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