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固体颗粒的化学性质对其在水溶液中电泳动电位的影响。

THE INFLUENCE OF THE CHEMICAL NATURE OF SOLID PARTICLES ON THEIR CATAPHORETIC P.D. IN AQUEOUS SOLUTIONS.

机构信息

Laboratories of The Rockefeller Institute for Medical Research.

出版信息

J Gen Physiol. 1923 Nov 20;6(2):215-37. doi: 10.1085/jgp.6.2.215.

Abstract
  1. The effect of eight salts, NaCl, Na(2)SO(4), Na(4)Fe(CN)(6), CaCl(2), LaCl(3), ThCl(4), and basic and acid fuchsin on the cataphoretic P.D. between solid particles and aqueous solutions was measured near the point of neutrality of water (pH 5.8). It was found that without the addition of electrolyte the cataphoretic P.D. between particles and water is very minute near the point of neutrality (pH 5.8), often less than 10 millivolts, if care is taken that the solutions are free from impurities. Particles which in the absence of salts have a positive charge in water near the point of neutrality (pH 5.8) are termed positive colloids and particles which have a negative charge under these conditions are termed negative colloids. 2. If care is taken that the addition of the salt does not change the hydrogen ion concentration of the solution (which in these experiments was generally pH 5.8) it can be said in general, that as long as the concentration of salts is not too high, the anions of the salt have the tendency to make the particles more negative (or less positive) and that cations have the opposite effect; and that both effects increase with the increasing valency of the ions. As soon as a maximal P.D. is reached, which varies for each salt and for each type of particles, a further addition of salt depresses the P.D. again. Aside from this general tendency the effects of salts on the P.D. are typically different for positive and negative colloids. 3. Negative colloids (collodion, mastic, Acheson's graphite, gold, and metal proteinates) are rendered more negative by low concentrations of salts with monovalent cation (e.g. Na) the higher the valency of the anion, though the difference in the maximal P.D. is slight for the monovalent Cl and the tetravalent Fe(CN)(6) ions. Low concentrations of CaCl(2) also make negative colloids more negative but the maximal P.D. is less than for NaCl; even LaCl(3) increases the P.D. of negative particles slightly in low concentrations. ThCl(4) and basic fuchsin, however, seem to make the negative particles positive even in very low concentrations. 4. Positive colloids (ferric hydroxide, calcium oxalate, casein chloride-the latter at pH 4.0) are practically not affected by NaCl, are rendered slightly negative by high concentrations of Na(2)SO(4), and are rendered more negative by Na(4)Fe(CN)(6) and acid dyes. Low concentrations of CaCl(2) and LaCl(3) increase the positive charge of the particles until a maximum is reached after which the addition of more salt depresses the P.D. again. 5. It is shown that alkalies (NaOH) act on the cataphoretic P.D. of both negative and positive particles as Na(4)Fe(CN)(6) does at the point of neutrality. 6. Low concentrations of HCl raise the cataphoretic P.D. of particles of collodion, mastic, graphite, and gold until a maximum is reached, after which the P.D. is depressed by a further increase in the concentration of the acid. No reversal in the sign of charge of the particle occurs in the case of collodion, while if a reversal occurs in the case of mastic, gold, and graphite, the P.D. is never more than a few millivolts. When HCl changes the chemical nature of the colloid, e.g. when HCl is added to particles of amphoteric electrolytes like sodium gelatinate, a marked reversal will occur, on account of the transformation of the metal proteinate into a protein-acid salt. 7. A real reversal in the sign of charge of positive particles occurs, however, at neutrality if Na(4)Fe(CN)(6) or an acid dye is added; and in the case of negative colloids when low concentrations of basic dyes or minute traces of ThCl(4) are added. 8. Flocculation of the suspensions by salts occurs when the cataphoretic P.D. reaches a critical value which is about 14 millivolts for particles of graphite, gold, or mastic or denatured egg albumin; while for collodion particles it was about 16 millivolts. A critical P.D. of about 15 millivolts was also observed by Northrop and De Kruif for the flocculation of certain bacteria.
摘要
  1. 在接近水的中性点(pH 值 5.8)处,测量了八种盐,即 NaCl、Na(2)SO(4)、Na(4)Fe(CN)(6)、CaCl(2)、LaCl(3)、ThCl(4)和碱性及酸性品红对固体质点和水溶液之间的电泳动电位的影响。结果发现,如果小心确保溶液中没有杂质,那么在没有电解质的情况下,质点与水之间的电泳动电位在中性点附近(pH 值 5.8)非常小,通常小于 10 毫伏。在中性点(pH 值 5.8)附近带有正电荷的质点被称为正胶体,而在这些条件下带负电荷的质点被称为负胶体。

  2. 如果小心确保盐的添加不会改变溶液的氢离子浓度(在这些实验中通常为 pH 值 5.8),那么可以一般地说,只要盐的浓度不是太高,盐的阴离子就有使质点带更多负电荷(或更少正电荷)的趋势,阳离子则有相反的效果;并且这两种效果都随着离子的化合价的增加而增加。一旦达到最大的 P.D.,它因每种盐和每种类型的质点而异,进一步添加盐会再次降低 P.D.。除了这种一般趋势外,盐对 P.D.的影响对于正胶体和负胶体来说是典型不同的。

  3. 负胶体(胶棉、乳香、艾奇逊石墨、金和金属蛋白酸盐)在低浓度的单价阳离子(例如 Na)盐的作用下变得更加负电,阴离子的化合价越高,尽管对于单价 Cl 和四价 Fe(CN)(6)离子,最大 P.D.的差异很小。低浓度的 CaCl(2)也使负胶体带更多负电,但最大 P.D.比 NaCl 低;甚至 LaCl(3)在低浓度下也会使负粒子的 P.D.略有增加。然而,ThCl(4)和碱性品红似乎使负粒子即使在非常低的浓度下也带正电。

  4. 正胶体(氢氧化铁、草酸钙、酪蛋白氯化物——后者在 pH 值 4.0 时)几乎不受 NaCl 的影响,在高浓度的 Na(2)SO(4)的作用下略带负电,并且在 Na(4)Fe(CN)(6)和酸性染料的作用下带更多负电。低浓度的 CaCl(2)和 LaCl(3)增加质点的正电荷,直到达到最大值,之后再添加更多的盐会再次降低 P.D.。

  5. 证明碱(NaOH)在中性点处对正胶体和负胶体的电泳动电位的影响与 Na(4)Fe(CN)(6)相同。

  6. 低浓度的 HCl 会增加胶棉、乳香、石墨和金质点的电泳动电位,直到达到最大值,之后再增加酸的浓度会降低 P.D.。在胶棉的情况下,不会发生质点电荷符号的反转,而在乳香、金和石墨的情况下,如果发生反转,P.D.也不会超过几个毫伏。当 HCl 改变胶体的化学性质时,例如当 HCl 被添加到两性电解质如钠明胶的质点中时,由于金属蛋白酸盐转化为蛋白酸盐,会发生明显的反转。

  7. 然而,在中性条件下,如果添加 Na(4)Fe(CN)(6)或酸性染料,正胶体的电荷符号会发生真正的反转;而对于负胶体,当添加低浓度的碱性染料或微量的 ThCl(4)时,也会发生反转。

  8. 当电泳动电位达到临界值时,盐会使悬浮液絮凝,对于石墨、金或乳香或变性卵白蛋白的质点,临界值约为 14 毫伏;而对于胶棉质点,临界值约为 16 毫伏。Northrop 和 De Kruif 也观察到某些细菌的絮凝临界值约为 15 毫伏。

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