Preparation method of propyl silane oligomer product

文档序号:1053098 发布日期:2020-10-13 浏览:9次 中文

阅读说明:本技术 一种丙基硅烷低聚物产品的制备方法 (Preparation method of propyl silane oligomer product ) 是由 刘明锋 阮少阳 吴兵兵 陈圣云 甘俊 甘书官 于 2020-07-28 设计创作,主要内容包括:本发明涉及一种丙基硅烷低聚物产品的制备方法,属精细化工技术领域。本发明以丙基烷氧基硅烷粗品(pH=7)、自来水为原料,浓盐酸为催化剂,三聚硫氰酸三钠盐为金属捕捉剂,醇为溶剂,采用水解、缩合工艺合成的丙基硅烷低聚物产品,因使用了三聚硫氰酸三钠盐金属捕捉剂,可以很好的去除丙基三氯硅烷溶解其腐蚀储罐及输送管道的金属离子,与丙基烷氧基硅烷产品水解合成丙基硅烷低聚物产品的合成方法相比,丙基烷氧基硅烷不需要蒸馏工序,不副产丙基烷氧基硅烷重组分,因此,本专利的合成方法既经济又环保,另外,合成的丙基硅烷低聚物产品成本低、价格低,可以向建筑防水材料领域全面推广,解决了丙基烷氧基硅烷带来的库存与环保问题。(The invention relates to a preparation method of propyl silane oligomer products, belonging to the technical field of fine chemical engineering. The invention takes propyl alkoxy silane crude product (pH = 7) and tap water as raw materials, concentrated hydrochloric acid as catalyst, trisodium trithiocyanate as metal trapping agent, alcohol as solvent, and adopts hydrolysis and condensation process to synthesize propyl silane oligomer product, because of using the trisodium trithiocyanate metal trapping agent, can well remove metal ions which are dissolved by the propyl trichlorosilane and corrode a storage tank and a conveying pipeline, compared with the synthesis method for synthesizing the propyl silane oligomer product by hydrolyzing the propyl alkoxy silane product, the propyl alkoxy silane does not need a distillation process and does not produce a byproduct of propyl alkoxy silane heavy components, so the synthesis method of the patent is economic and environment-friendly, in addition, the synthesized propyl silane oligomer product has low cost and low price, can be comprehensively popularized to the field of building waterproof materials, and solves the problems of inventory and environmental protection brought by propyl alkoxy silane.)

1. A process for the preparation of a propyl silane oligomer product, comprising the steps of:

1) the method comprises the following steps of adding a crude propyl alkoxysilane (pH = 7), trisodium trithiocyanate and a solvent into a four-neck flask connected with a reflux condenser (connected with a cooling circulating water device) and a thermometer, and adding tap water, the solvent and a hydrochloric acid catalyst into a constant-pressure dropping funnel connected with the four-neck flask, wherein the mass ratio of the trisodium trithiocyanate to the crude propyl alkoxysilane is 0.5-1%: 1, the molar ratio of tap water to the crude propyl alkoxysilane is 0.8: 1, the ratio of the crude propyl alkoxy silane to the solvent in the four-neck flask is 3.0: 1, the mass ratio of tap water to solvent in the constant-pressure funnel is 1: 1, the hydrochloric acid catalyst is 0.05-0.1% of a crude product of propyl alkoxy silane;

2) after the material preparation is finished, opening a magnetic stirrer, starting a constant-temperature heating device, slowly and uniformly dropping a mixture material in a constant-pressure dropping funnel into a four-neck flask to perform hydrolysis reaction and hydroxyl condensation reaction after the temperature of a kettle reaches 60 ℃, and controlling the temperature of the kettle to be 60-70 ℃ in the hydrolysis reaction process;

3) after the dropwise addition of the mixed materials is finished, controlling the temperature of the kettle to be 60-70 ℃, and carrying out an aging reaction for 2 hours to ensure that the tap water reacts completely;

4) after the reaction is finished, gradually heating the four-neck flask to raise the temperature, and evaporating the solvent in the four-neck flask until the solvent is distilled;

5) after the solvent distillation is finished, reducing the temperature of a kettle of the four-mouth flask to 50-60 ℃, then adding a proper amount of decolorant into the flask to decolor and adsorb, gradually heating the four-mouth flask to decolor and adsorb, wherein the decoloring and adsorbing time is 5 hours, and the temperature of the kettle in the whole process of decoloring and adsorbing is controlled to be 110-120 ℃;

6) and after the decoloring and adsorption processes are finished, cooling the kettle in the four-neck flask to room temperature, and filtering to obtain a colorless and transparent propyl silane oligomer product.

Technical Field

The invention relates to a preparation method of propyl silane oligomer products, belonging to the technical field of fine chemical engineering.

Background

In recent years, silane monomolecular derivative oligomers have the characteristics of low VOC, strong bonding, high boiling point, low volatility, high crosslinking, low dosage, yellowing resistance, good water resistance and the like, and are widely used in the fields of coatings, adhesives, sealants, plastics, powder, metals, water resistance and the like, so the research on the silane derivative oligomerization technology is widely concerned at home and abroad, functional siloxane oligomers (also called silane oligomers) are functional organic silicon polymers with low viscosity, few chain segments and high functionality formed by hydrolysis/condensation of one or more than two silane coupling agents, modified organic polymers of the functional siloxane oligomers have excellent compatibility and molecular controllability, the heat resistance, impact resistance, bonding, lubrication, flame retardance, pollution resistance, wear resistance, solvent resistance, air permeability and the like of polymer materials can be obviously improved, for example, aminoalkyl block copolymer oligomeric siloxanes not only show excellent wettability to material interfaces, and can form chemical bonds with the interface of materials difficult to be adhered, which have strong weather resistance and moisture resistance, wherein amino groups provide chemical fields capable of reacting with active matrix polymers, and alkyl groups impart excellent hydrophobicity, so that it is widely used in paints, adhesives, sealants and the like to improve the adhesion and wettability with inorganic surfaces, plastic surfaces.

At present, organosilicone waterproofing agents are widely researched and applied to building waterproofing materials, alkyl silicate organosilicone waterproofing agents such as methyl sodium silicate, ethyl sodium silicate and phenyl sodium silicate which are widely used in the market can be condensed into a waterproofing membrane under the action of water and CO2, the waterproofing membrane surrounds particles of concrete, so that the base material is hydrophobic, free access of water vapor is not hindered, the air permeability of the base material is ensured, the impermeability and the durability are improved, other performances of the base material cannot be improved, the silicate is a water-soluble polymer with low molecular weight, the silicate can run off along with the washing of rainwater, and the hydrophobicity can lose within months or two years. On the other hand, in industrial production, the production of by-products of 20% by mass of the product is accompanied, and the demand is rapidly increasing with the expansion of the application field thereof, thereby leading to the occurrence of a large amount of by-products, the main components of which are tetraalkoxysilane and propylalkoxysilane, which can be sold, and the propylalkoxysilane which is small in the market and cannot be completely sold.

Disclosure of Invention

The invention aims to: the preparation method of the propyl silane oligomer product is economic and environment-friendly, and the synthesized product can be comprehensively popularized to the field of building waterproof materials and can realize industrial production.

The technical scheme of the invention is as follows:

a process for the preparation of a propyl silane oligomer product, comprising the steps of:

1) the method comprises the following steps of adding a crude propyl alkoxysilane (pH = 7), trisodium trithiocyanate and a solvent into a four-neck flask connected with a reflux condenser (connected with a cooling circulating water device) and a thermometer, and adding tap water, the solvent and a hydrochloric acid catalyst into a constant-pressure dropping funnel connected with the four-neck flask, wherein the mass ratio of the trisodium trithiocyanate to the crude propyl alkoxysilane is 0.5-1%: 1, the molar ratio of tap water to the crude propyl alkoxysilane is 0.8: 1, the ratio of the crude propyl alkoxy silane to the solvent in the four-neck flask is 3.0: 1, the mass ratio of tap water to solvent in the constant-pressure funnel is 1: 1, the hydrochloric acid catalyst is 0.05 to 0.1 percent of crude propyl alkoxy silane,

2) after the material preparation is finished, opening a magnetic stirrer, starting a constant-temperature heating device, slowly and uniformly dropping a mixture material in a constant-pressure dropping funnel into a four-neck flask to perform hydrolysis reaction and hydroxyl condensation reaction after the temperature of a kettle reaches 60 ℃, and controlling the temperature of the kettle to be 60-70 ℃ in the hydrolysis reaction process;

3) after the dropwise addition of the mixed materials is finished, controlling the temperature of the kettle to be 60-70 ℃, and carrying out an aging reaction for 2 hours to ensure that the tap water reacts completely;

4) after the reaction is finished, gradually heating the four-neck flask to raise the temperature, and evaporating the solvent in the four-neck flask until the solvent is distilled;

5) after the solvent distillation is finished, reducing the temperature of a kettle of the four-mouth flask to 50-60 ℃, then adding a proper amount of decolorant into the flask to decolor and adsorb, heating the four-mouth flask gradually to decolor and adsorb, wherein the decoloring and adsorbing time is 5 hours,

6) and after the decoloring and adsorption processes are finished, cooling the kettle in the four-neck flask to room temperature, and filtering to obtain a colorless and transparent propyl silane oligomer product.

The reaction equation of the present invention is as follows:

5C3H7Si(OR)3+ 4H2O → RO[C3H7Si(OR)O]5R+ 8ROH

in the formula, R is a hydrocarbyl group such as methyl, ethyl, isopropyl and the like.

In order to verify the influence of the whole process of catalyst and decoloration and adsorption on the product quality, the inventor carries out a comparative test, and the result is as follows:

table 1: influence of catalyst feed ratio on the product:

Figure 469246DEST_PATH_IMAGE001

table 2: the kettle temperature in the whole decoloring and adsorption process is controlled to be 110-120 ℃, and the influence of the decoloring kettle temperature on the product quality is as follows:

Figure 780141DEST_PATH_IMAGE002

the invention has the following effects:

the invention takes propyl alkoxy silane crude product (pH = 7) and tap water as raw materials, concentrated hydrochloric acid as catalyst, trisodium trithiocyanate as metal trapping agent, alcohol as solvent, and adopts hydrolysis and condensation process to synthesize propyl silane oligomer product, because of using the trisodium trithiocyanate metal trapping agent, can well remove metal ions which are dissolved by the propyl trichlorosilane and corrode a storage tank and a conveying pipeline, compared with the synthesis method for synthesizing the propyl silane oligomer product by hydrolyzing the propyl alkoxy silane product, the propyl alkoxy silane does not need a distillation process and does not produce a byproduct of propyl alkoxy silane heavy components, so the synthesis method of the patent is economic and environment-friendly, in addition, the synthesized propyl silane oligomer product has low cost and low price, can be comprehensively popularized to the field of building waterproof materials, and solves the problems of inventory and environmental protection brought by propyl alkoxy silane.

Detailed Description

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