Abstract:
Preparation of polyisobutylene having a content of terminal double bonds of more than 50% by polymerizing isobutene using a polymerization catalyst customary therefor from a technical 1-butene-, 2-butene- and isobutene-containing C4 hydrocarbon stream which may comprise up to 3000 ppm by weight, of 1,3-butadiene, by reducing the content of oxygenates in the C4 hydrocarbon stream before the polymerization of the isobutene by contacting it with an inorganic adsorbent at a pressure of from 1 to 20 bar and a temperature of from 20 to 220° C.
Abstract:
The invention relates to a process for preparing polyisobutene having a mean molecular weight Mn of from 400 to 50 000, in particular from 500 to 10 000, by polymerizing isobutene in the presence of a BF3-containing complex catalyst, wherein the polymerization is carried out at least temporarily in the presence of one or more cyclic ethers.
Abstract:
A process is described for epoxidizing an ethylenically unsaturated isobutene polymer, in which an organic phase comprising the isobutene polymer is contacted with an aqueous phase which comprises formic acid and hydrogen peroxide. The process affords essentially quantitative conversions after a short reaction time.
Abstract:
The invention relates to a method for producing mainly ethylenically unsaturated isobutene polymers, wherein the sum of proportions of molecules with a double bond in an α position and molecules with a double bond in a position β is increased to 75% mol by polymerising isobutene in a liquid phase in the presence of a diluted or dispersed catalyst complex which comprises (i) an electron donor and (ii) a compound of general formula (I) HaMeb[MFx]c, wherein Me is a metal with oxidation state m, M is an element selected from elements of the groups 2, 3, 4, 5, 10, 11, 13, 14 or 15 of the periodic table according to the IUPAC notation of an element oxidation number n, a is an integer ≧1, b is an integer ≧0, x is an integer ≧2 and c is [(a+mb)/(x−n)]. The catalyst is preferably embodied in the form of HBF4O(CH3)2. The inventive method makes it possible to obtain an isobutene polymer having a low fluorine-content even using technical C4 hydrocarbon portions as an isobutene source.
Abstract:
The invention describes polyisobutenyl derivatives of succinic acid obtainable by: i) reacting a polyisobutene which has a reactive end group content of at least 80% and whose molecular weight distribution is characterized by a maximum MP in the distribution curve in the range from 500 to 20 000 daltons and a ratio of weight average molecular weight to number average molecular weight MW/MN of below 1.4 with maleic acid or maleic anhydride; ii) reacting the polyisobutene-succinic acid derivative obtained in i) with at least one compound I which has at least one primary or secondary amino group and/or an OH group to form an amide or ester bond, and also a process for preparing them and their use as additives in lubricant compositions.
Abstract translation:本发明描述了琥珀酸的聚异丁烯基衍生物,其可通过以下方式获得:i)使具有至少80%的反应性末端基团含量的聚异丁烯反应,其分子量分布的特征在于分布中的最大M P 曲线范围为500至20,000道尔顿,重均分子量与数均分子量M的比值低于1.4,与马来酸或马来酸酐 酐; ii)使i)中得到的聚异丁烯 - 琥珀酸衍生物与至少一种具有至少一个伯或仲氨基和/或OH基团的化合物I反应形成酰胺键或酯键,以及制备它们的方法 以及它们作为润滑剂组合物中的添加剂的用途。
Abstract:
The present invention relates to a process for preparing an isobutene polymer using a cyclopentene derivative as initiator and to the isobutene polymer obtainable by means of the process and to particular functionalization products thereof.
Abstract:
Thermal reaction products of maleic anhydride and oligoalkenes are obtainable by oligomerization of linear C8- to C12-1-alkenes, preferably in the presence of a titanium, zirconium or hafnium metallocene catalyst and of an activator based on organoaluminum, organoboron or carbocationic compounds and have a vinylidene double bond content of more than 30% and have a number average molecular weight from 1000 to 20,000. Derivatives thereof with amines or alcohols are used as fuel additives and lubricant additives.
Abstract:
Reaction products of polyolefins having predominantly a terminal double bond and a number average molecular weight of from 250 to 10,000, which possess an aliphatic hydrocarbon skeleton which is straight-chain or carries C.sub.1 -C.sub.4 -alkyl side chains, with from 1 to 10 mol, per equivalent of double bond, of one or more vinyl esters I ##STR1## are obtainable by reacting the stated polyolefins with the vinyl esters I in the presence of a free radical initiator at from 80 to 200.degree. C., it being possible for these reaction products subsequently to have been hydrolyzed to the corresponding alcohols or converted into the corresponding amines by reductive amination with amines II ##STR2## .