Havingbrieflyexaminedthestructureoforganicpackingsandthevariousroutesintheirmanufacture,themostimportantfeaturesmaybesummarizedasfollows:>Hydrophilicaswellaslipophilicorg... Having briefly examined the structure of organic packings and the various routes
in their manufacture, the most important features may be summarized as follows:
> Hydrophilic as well as lipophilic organic packings are synthesized with a controlled
pore and surface structure depending on the type of monomer/comonomer
and the polymerization reaction. Surface structure can be altered by
controlled consecutive surface reactions.
> In accordance with the bulk composition, polymer packings are stable across
almost the entire pH range, particularly under strong alkaline conditions.
> Chemical stability is affected by oxidizing and reducing solutions.
> Although cross-linking reactions have been optimised in as much as rigid pressure
stable particles can be manufactured, some remaining swelling property is
often noted when changing the solvent composition in HPLC.
> As in the manufacture of silica, porosity, pore size, and surface area of polymer
packings can be adjusted over a wide range, and micro-, meso-, and macro- as well
as non-porous beads are synthesized reproducibly.
3.2.4.2 Hydrophobic Polymer Stationary Phases
The synthesis of cross-linked copolymers of styrene and divinylbenzene has been
studied intensively and is well documented. The starting monomer is styrene, and
divinylbenzene (DVB) is used as cross-linker. The amount of DVB can reach up to
55wt.%. At 55% DVB, the copolymer shows practically no swelling and possesses a
permanent porosity. Figure 3.21 illustrates the network structure of poly(styrenedivinylbenzene)
(St-DVB).
Commercial products differ in bead size and pore size. There are even non-porous
products on the market, designed for the rapid separation of peptides and proteins
by reversed phase HPLC (Maa and Horvath, 1988). St-DVB copolymers are stable in
the pH range 0–14. They find increasing application in the separation of low molecular
weight compounds, peptides, and proteins by means of reversed phase chromatography
(Tanaka et al., 1987, Tweeten and Tweeten, 1986) and as parent materials
for the synthesis of derivatized packings in interaction chromatography of biopoly-mers (Unger et al., 1987, Regnier, 1987). Numerous other organophilic polymer
packings have been synthesized for size exclusion and interactive HPLC after suitable
derivatization. They are reviewed in depth by Mikes (1988).
简单的结构有了有机包装,不同的路线
在他们的制造、Z重要的特征可归纳如下:
>亲水性以及合成有机包装亲与控制
毛孔及表面结构的负载量单体/单体含量
和聚合反应。能够改变表面结构
连续控制表面的反应。
根据大多数>组成、聚合物填料是稳定的理解
几乎整个pH范围,特别是在强碱性条件下。
>的化学稳定性是受氧化性和减少的解决方案。
>虽然交联反应被优化一样,作为刚性的压力
我们可以生产稳定粒子,有些剩下的肿胀财产
经常注意变更溶剂成分在GX液相色谱。
在生产》和白炭黑、孔隙度、孔径、和表面面积的聚合物
包装可在一范围内自由调整——、中观和微观3 -,和宏观-
可以作为合成珠子层。
3.2.4.2疏水性聚合物固定阶段
交联共聚物的合成、苯乙烯、divinylbenzene的
深入钻研了和有明文规定。开始单体苯乙烯、
divinylbenzene(DVB),是用来作为调控涂饰剂。数字移动电视的数量可达
55wt. %。对他们来说很有效果DVB、共聚物几乎没有肿胀,拥有了
的孔隙度。图3.21说明了网络结构对聚酯styrenedivinylbenzene)
(St-DVB)。
珠大小不同的商业产品和孔径。甚至有层
产品在市场上,设计的快速多肽和蛋白质的分离
通过反相GX液相色谱法(共和Horvath,1988)。St-DVB共聚物是稳定的
0-14 pH范围。他们发现越来越多地应用低分子分离
重量肽段和蛋白质的化合物,通过反相色谱
(田中、苏达权等,1987年,Tweeten和Tweeten,1986年),作为父母的材料
结果的综合作用色谱填料biopoly-mers(Unger苏达权等,1987年,Regnier,1987)。不计其数的其他organophilic聚合物
合成了包装大小排斥和互动GX液相色谱(HPLC)经过合适的
derivatization。他们等方面的研究进展,麦克一家深度(1988)。