Разработка композиции на основе полимочевины с увеличенным сроком жизни

Objectives. Improvement of the technology for obtaining polymer-sprayed coatings based on polycarbodiimides (polyureas) with high chemical, hydrolytic, and abrasive resistance and improved physical and mechanical properties, as well as obtainment of polyurea compositions with a lifetime of at least 5 min without loss performance characteristics (i.e., “hand-applied” polyureas) suitable for repair of coatings already in use.Methods. The reaction rate between isocyanate and amino groups is almost a hundred times higher than that between isocyanate and hydroxyl groups, necessitating the use of special highperformance and high-pressure installations equipped with self-cleaning mixing chambers and heating of components. The following are determined from the obtained materials: strength, elongation at break according to the standard method, Taber abrasion, and Shore hardness.Results. Three methods of slowing down the reaction are investigated: 1) the synthesis of prepolymers with the content of NCO groups from 10.5% to 18%; 2) the addition of a plasticizer into the prepolymer in the amount of 1–10 mass parts; and 3) the introduction of polyesters into the composition and radiation of the so-called “hybrid” systems. When using 14% polyesters with a molecular weight of 2000 Da, only “hybrid” systems make it possible to obtain compositions with a lifetime of more than 5 min. At the same time, the tensile strength decreases by 20%, and the abrasion increases by 40%; however, such “hybrid” systems have a higher adhesion force and are cheaper than pure polyureas, allowing them to be used as “repair” systems.Conclusions. The developed composition and technology of applying “hybrid” systems allow for the repair of existing coatings without using specialized devices. “Manual” polyurea is easy to use and does not require special training. Цели. Совершенствование технологии получения полимерных напыляемых покрытий на основе поликарбодиимидов (полимочевин), с высокой химической, гидролитической и абразивной стойкостью и улучшенными физико-механическими показателями, а также, получение полимочевинных композиций с временем жизни не менее 5 мин без потери эксплуатационных характеристик (полимочевин «ручного» нанесения), пригодных для ремонта уже эксплуатирующихся покрытий.Методы. Скорость реакции между изоцианатными и аминогруппами практически в сто раз превышает скорость реакции между изоцианатными и гидроксильными группами, что вызывает необходимость использовать специальные высокопроизводительные установки высокого давления, оснащенные самоочищающимися смесительными камерами и обогревом компонентов. У полученных материалов определяли прочность, удлинение на разрыв по стандартной методике, истираемость по Таберу и твердость по Шору.Результаты. Исследованы три способа замедления реакции: во-первых, синтез предполимеров с содержанием NCO-групп от 10.5% до 18%; во-вторых, введение в предполимер пластификатора в количестве 1–10 масс.ч.; в-третьих, введение в композицию полиэфиров и получения «гибридных» систем. Показано, что только «гибридные» системы при использовании полиэфиров с молекулярной массой 2000 Да, в количестве 14% позволяют получить композиции с временем жизни более 5 мин. При этом прочность на разрыв снижается на 20%, истираемость увеличивается на 40%, но такие «гибридные» системы имеют более высокую силу адгезии и дешевле по сравнению с чистыми полимочевинами, что позволяет использовать их в качестве «ремонтных» систем.Выводы. Разработанный состав и технология нанесения «гибридных» систем позволяют производить ремонтные работы существующих покрытий без применения специализированных устройств. Полимочевина «ручного» нанесения удобна в эксплуатации и не требует специальной подготовки.

Drosophila Dynein Intermediate Chain Gene, Dic61B, Is Required for Spermatogenesis

This study reports the identification and characterization of a novel gene, Dic61B, required for male fertility in Drosophila. Complementation mapping of a novel male sterile mutation, ms21, isolated in our lab revealed it to be allelic to CG7051 at 61B1 cytogenetic region, since two piggyBac insertion alleles, CG7051c05439 and CG7051f07138 failed to complement. CG7051 putatively encodes a Dynein intermediate chain. All three mutants, ms21, CG7051c05439 and CG7051f07138, exhibited absolute recessive male sterility with abnormally coiled sperm axonemes causing faulty sperm individualization as revealed by Phalloidin staining in Don Juan-GFP background. Sequencing of PCR amplicons uncovered two point mutations in ms21 allele and confirmed the piggyBac insertions in CG7051c05439 and CG7051f07138 alleles to be in 5′UTR and 4th exon of CG7051 respectively, excision of which reverted the male sterility. In situ hybridization to polytene chromosomes demonstrated CG7051 to be a single copy gene. RT-PCR of testis RNA revealed defective splicing of the CG7051 transcripts in mutants. Interestingly, expression of cytoplasmic dynein intermediate chain, α, β, γ tubulins and α-spectrin was normal in mutants while ultra structural studies revealed defects in the assembly of sperm axonemes. Bioinformatics further highlighted the homology of CG7051 to axonemal dynein intermediate chain of various organisms, including DNAI1 of humans, mutations in which lead to male sterility due to immotile sperms. Based on these observations we conclude that CG7051 encodes a novel axonemal dynein intermediate chain essential for male fertility in Drosophila and rename it as Dic61B. This is the first axonemal Dic gene of Drosophila to be characterized at molecular level and shown to be required for spermatogenesis

Features of Phase Formation in the CsOH–H₂SO₄–H₃PO₄–H₂O System and the Growth of the Cs₆(SO₄)₃(H₃PO₄)₄ Crystals

In this paper, the conditions of phase formation in the system CsOH–H2SO4–H3PO4–H2O are considered for the first time. The phase formation of Cs6(SO4)3(H3PO4)4 at t = 50 °C has been studied extensively. The main concentration boundary conditions for this compound are considered for the first time. The solubility congruence of Cs6(SO4)3(H3PO4)4 is shown. Conditions and approaches for obtaining crystals by isothermal evaporation and saturated solution temperature reduction methods are considered. The results of obtaining Cs6(SO4)3(H3PO4)4 crystals with maximum dimensions of ~20 mm are presented