Termooxidaition destruction of butadiene-nitrile rubbers and industrial waste

T. N. Shehavtsova, G. V. Shatalov, V. N. Papkov, O. Karmanova
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Abstract

The process of thermooxidation destruction of industrial butadiene-nitrile copolymers of the grades SKN-18, SKN-26 and substandard products is investigated. The process is carried out in aromatic solvents (toluene in the xylene) under the influence of air oxygen in the presence of an adduct of the radical initiator azodiisobutyronitrile with N-metilpirrolidone. The mass-average molecular weights of the resulting products were determined by gel permeation chromatography, and molecular weight distribution calculations were performed. The influence of the temperature and the content of the initiator on the change in the intrinsic viscosity of solutions of the resulting degradation products, depending on the time of the process, is considered. Based on a comparative analysis of the destruction parameters using toluene and xylene at 80 °C and an initiator concentration of 0.8% by weight. It was found that the type of solvent and the time of destruction practically do not affect the process of thermooxidative destruction with the production of low molecular weight polymers with a molecular weight of 40 ? 103. It is shown that in the course of the destruction of industrial rubbers differing in the content of acrylonitrile, the process proceeds with the formation of higher molecular weight compounds in rubbers with a higher content of acrylonitrile units. When carrying out the destruction of substandard rubber SKN-26SNT with high Defoe hardness, it is necessary to increase the concentration of the initiator to 1.1% of the mass. and temperature. The mechanism of thermooxidative destruction of the studied polymers is considered. According to the data of IR spectroscopy and chemical analysis, it was found that the products of thermooxidative destruction of nitrile butadiene rubbers contain oxygen-containing functional groups. Thus, a simple commercially method for producing low-molecular-weight butadiene-nitrile polymers based on special-purpose rubbers and substandard product with functional hydroxyl, carboxyl and epoxy groups has been developed.
丁腈橡胶和工业废料的热氧化破坏
研究了SKN-18、SKN-26级工业丁腈共聚物及不合格品的热氧化破坏过程。该过程在芳香溶剂(二甲苯中的甲苯)中进行,在自由基引发剂偶氮二异丁腈与n -甲吡咯烷酮的加合物存在下,在空气氧的影响下进行。通过凝胶渗透色谱法测定产物的质量平均分子量,并进行分子量分布计算。考虑了温度和引发剂含量对降解产物溶液特性粘度随时间变化的影响。通过对甲苯和二甲苯在80℃、引发剂质量分数为0.8%条件下的破坏参数进行对比分析。结果表明,溶剂类型和破坏时间对热氧化破坏过程几乎没有影响,制备的低分子量聚合物分子量为40 ?103. 结果表明,在丙烯腈含量不同的工业橡胶的破坏过程中,丙烯腈单位含量较高的橡胶中会形成分子量较高的化合物。对高笛福硬度的不合格橡胶SKN-26SNT进行破坏时,需要将引发剂的浓度提高到质量的1.1%。和温度。讨论了所研究聚合物的热氧化破坏机理。根据红外光谱和化学分析数据,发现丁腈橡胶热氧化破坏产物中含有含氧官能团。因此,开发了一种以特殊用途橡胶和含官能团羟基、羧基和环氧基的不合格产品为基础生产低分子量丁腈聚合物的简单商业方法。
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