POLYESTERS CONTAINING COPOLYMERIZED SUBSTITUTED 1,4-BIS(2,6-DIALKYLANILINO)-9,10-ANTHRAQUINONES AS COLORANTS
    232.
    发明申请
    POLYESTERS CONTAINING COPOLYMERIZED SUBSTITUTED 1,4-BIS(2,6-DIALKYLANILINO)-9,10-ANTHRAQUINONES AS COLORANTS 审中-公开
    含有共轭取代的1,4-BIS(2,6-二氯氰基)-9,10-蒽醌的聚酯作为颜料

    公开(公告)号:WO1998014502A1

    公开(公告)日:1998-04-09

    申请号:PCT/US1997017100

    申请日:1997-09-30

    CPC classification number: C08G63/6856 C08G63/68 C08L101/00 C08L67/02

    Abstract: A colored polyester copolymer comprising the reaction product of at least one linear thermoplastic polyester precursor and at least ten parts per million by weight of a residue of at least one 1,4-bis(2,6-dialkylanilino)-9,10-anthraquinone colorant. A composition may be formed comprising the copolymer in admixture with at least one thermoplastic polymer. The copolymer may be formed by reacting at least one thermoplastic polyester precursor with a 1,4-bis(2,6-dialkylanilino)-9,10-anthraquinone colorant which has a polyester reactive group.

    Abstract translation: 一种着色的聚酯共聚物,其包含至少一种直链热塑性聚酯前体和至少十份(重量)至少一种1,4-二(2,6-二烷基苯胺基)-9,10-蒽醌的残余物的反应产物 着色剂。 可以形成包含共聚物与至少一种热塑性聚合物混合的组合物。 共聚物可以通过使至少一种热塑性聚酯前体与具有聚酯反应性基团的1,4-双(2,6-二烷基苯胺基)-9,10-蒽醌着色剂反应形成。

    PROCESS FOR THE CONVERSION OF 2,3-DIHYDROFURAN TO CYCLOPROPANECARBOXALDEHYDE
    233.
    发明申请
    PROCESS FOR THE CONVERSION OF 2,3-DIHYDROFURAN TO CYCLOPROPANECARBOXALDEHYDE 审中-公开
    2,3-二氢呋喃转化为环丙烷氧基甲醛的方法

    公开(公告)号:WO1998008796A1

    公开(公告)日:1998-03-05

    申请号:PCT/US1997014546

    申请日:1997-08-19

    CPC classification number: C07C45/59 C07C47/293

    Abstract: Disclosed is a process for the preparation of cyclopropanecarboxaldehyde by the isomerization of 2,3-dihydrofuran wherein 2,3-dihydrofuran is contacted with a catalyst selected from alumina, silica-alumina, silica, zirconia, titania and mixtures thereof having a nitrogen BET surface area of 10 to 350 square meters per gram at elevated temperature.

    Abstract translation: 公开了通过2,3-二氢呋喃的异构化制备环丙烷甲醛的方法,其中2,3-二氢呋喃与选自氧化铝,二氧化硅 - 氧化铝,二氧化硅,氧化锆,二氧化钛及其混合物的催化剂接触,其具有氮BET表面 面积在升高的温度下为10至350平方米/克。

    PROCESS FOR FLUID/DENSE GAS EXTRACTION UNDER ENHANCED SOLUBILITY CONDITIONS
    234.
    发明申请
    PROCESS FOR FLUID/DENSE GAS EXTRACTION UNDER ENHANCED SOLUBILITY CONDITIONS 审中-公开
    在增强溶解条件下进行流体/渗透气体萃取的方法

    公开(公告)号:WO1998008584A1

    公开(公告)日:1998-03-05

    申请号:PCT/US1997015177

    申请日:1997-08-28

    CPC classification number: B01D11/0203 B01D11/0407

    Abstract: A liquid/dense gas extraction column process providing intimate contact between a dense gas and a fluid feed containing a solute and operating in an enhanced solubility region provides solubility of a solute in the dense gas to be at least 250 % by weight greater than the solubility of the solute in the dense gas at the same operating temperature and 200 bar pressure. The enhanced solubility region for carbon dioxide is a pressure range of between 450 and 1200 bar in combination with a temperature range between 50 and 300 DEG C. The column has a diameter greater than about 3.5 centimeters and a height to diameter ratio greater than about 5.

    Abstract translation: 提供致密气体和含有溶质并且在增强的溶解度区域中运行的流体进料之间的紧密接触的液体/致密气体提取柱方法提供致密气体中的溶质的溶解度至少比溶解度的250重量% 在相同的工作温度和200巴压力下的致密气体中的溶质。 二氧化碳的增强的溶解度区域在450和1200巴之间的压力范围以及在50和300℃之间的温度范围内组合。该柱具有大于约3.5厘米的直径,并且高度与直径之比大于约5 。

    ON-LINE QUANTITATIVE ANALYSIS OF CHEMICAL COMPOSITIONS BY RAMAN SPECTROMETRY
    235.
    发明申请
    ON-LINE QUANTITATIVE ANALYSIS OF CHEMICAL COMPOSITIONS BY RAMAN SPECTROMETRY 审中-公开
    通过拉曼光谱测定化学成分的在线定量分析

    公开(公告)号:WO1998008066A1

    公开(公告)日:1998-02-26

    申请号:PCT/US1996013530

    申请日:1996-08-22

    CPC classification number: G01J3/44 C08F2400/02 G01J2003/2866 G01N2201/1293

    Abstract: A method for quantitatively monitoring in situ by Raman spectrometry one or more selected constituents of a chemical composition comprises: simultaneously irradiating with a substantially monochromatic radiation source a reference material and a chemical composition containing one or more constituents, the radiation being transmitted from the source to the chemical composition by an excitation conduit connecting the source to an optical probe that interfaces with the composition; simultaneously acquiring at more than one wavelength convolved Raman spectra of the reference material and the chemical composition by means of a spectrograph, which is connected to the optical probe by a collection conduit; choosing the standard Raman spectrum of the reference material; determining the convolution function of the convolved spectra from the convolved Raman spectrum and the standard Raman spectrum of the reference material; applying the convolution function to adjust the convolved Raman spectrum of the composition to produce the standard Raman spectrum of the chemical composition; and applying predetermined calibration means to the standard Raman spectrum of the chemical composition, by which the chemical constitution of the composition at the time of acquisition of the convolved Raman spectra can be ascertained.

    Abstract translation: 用于通过拉曼光谱法原位定量监测化学成分的一种或多种所选成分的方法包括:同时向基本上单色的辐射源照射参考物质和含有一种或多种成分的化学组合物,所述辐射从源发射到 通过将源连接到与组合物接合的光学探针的激发导管的化学组成; 通过采集管连接到光学探针的光谱仪同时获取参考材料的多于一个波长卷积拉曼光谱和化学成分; 选择参考物质的标准拉曼光谱; 确定来自卷积拉曼光谱和参考物质的标准拉曼光谱的卷积光谱的卷积函数; 应用卷积函数调整组合物的卷积拉曼光谱,以产生化学成分的标准拉曼光谱; 并将预定的校准装置应用于化学组成的标准拉曼光谱,由此可以确定在获得卷积拉曼光谱时的组成的化学组成。

    PROCESS FOR IMPROVING THE FLAVOR RETAINING PROPERTY OF POLYESTER/POLYAMIDE BLEND CONTAINERS FOR OZONATED WATER
    236.
    发明申请
    PROCESS FOR IMPROVING THE FLAVOR RETAINING PROPERTY OF POLYESTER/POLYAMIDE BLEND CONTAINERS FOR OZONATED WATER 审中-公开
    用于改善臭氧水聚酯/聚酰胺混合容器的挥发性保持性能的方法

    公开(公告)号:WO1998007786A1

    公开(公告)日:1998-02-26

    申请号:PCT/US1997014521

    申请日:1997-08-19

    Abstract: The present invention relates to a process for minimizing the formation of undesirable byproducts in ozonated liquids comprising the steps of providing a container comprising a polyester comprising repeat units from a dicarboxylic acid component comprising at least about 85 mole percent terephthalic acid, 2,6-naphthalenedicarboxylic acid or a mixture thereof and at least about 85 mole percent ethylene glycol, and from about - to about - weight % of at least one polyamide which displays a melting point below that of said polyester, and filling said container with an ozonated liquid.

    Abstract translation: 本发明涉及一种使臭氧化液体中不期望的副产物形成最小化的方法,包括以下步骤:提供包含聚酯的容器,所述聚酯包含由二羧酸组分重复单元,所述二羧酸组分包含至少约85摩尔%的对苯二甲酸,2,6-萘二羧酸 酸或其混合物,和至少约85摩尔%的乙二醇和约 - 约重量%的至少一种聚酰胺,其显示熔点低于所述聚酯的熔点,并用臭氧化液体填充所述容器。

    PROCESS FOR THE SEPARATION OF 2-ALKENE-1,4-DIOLS AND 3-ALKENE-1, 2-DIOLS FROM CATALYSTS
    237.
    发明申请
    PROCESS FOR THE SEPARATION OF 2-ALKENE-1,4-DIOLS AND 3-ALKENE-1, 2-DIOLS FROM CATALYSTS 审中-公开
    2-烷基-1,4-二醇和3-烷基-1,2-二醇从催化剂中分离的方法

    公开(公告)号:WO1998002405A1

    公开(公告)日:1998-01-22

    申请号:PCT/US1997012384

    申请日:1997-07-16

    CPC classification number: C07C29/86 C07C29/88 C07C33/035

    Abstract: This invention provides a catalyst recovery process whereby a liquid/liquid extraction is used to separate mixtures of 2-alkene-1,4-diols and 3-alkene-1,2-diols, formed by the hydration of gamma,delta-epoxyalkenes using mixtures of hydriodic acid and organic solvent soluble iodide salts as catalysts, from the catalyst. In this extraction, gamma,delta-epoxyalkene, or a gamma,delta-epoxyalkene-containing organic solvent, is used to convert any hydriodic acid present to iodoalcohol and to extract the catalysts from water, leaving the diol products in the aqueous phase, from which they may be subsequently recovered by distillation, extraction or by other means.

    Abstract translation: 本发明提供一种催化剂回收方法,其中使用液/液萃取来分离通过γ,δ-环氧烯烃的水合形成的2-烯烃-1,4-二醇和3-烯烃-1,2-二醇的混合物,其使用 作为催化剂的氢碘酸和有机溶剂可溶性碘盐的混合物。 在该提取中,使用γ,δ-环氧化烯或含有γ-环氧烯烃的有机溶剂,将存在的任何氢碘酸转化为碘醇,并从水中提取催化剂,使二醇产物在水相中,从 它们可以随后通过蒸馏,萃取或其它方式回收。

    COMPOSITE FIBROUS STRUCTURES FOR ABSORPTION OF LIQUIDS
    238.
    发明申请
    COMPOSITE FIBROUS STRUCTURES FOR ABSORPTION OF LIQUIDS 审中-公开
    用于吸收液体的复合纤维结构

    公开(公告)号:WO1997043480A1

    公开(公告)日:1997-11-20

    申请号:PCT/US1997008068

    申请日:1997-05-08

    CPC classification number: D06M15/227 D06B1/10 D06M15/263 D06M2200/00

    Abstract: A composite fibrous structure which absorbs liquids is in the form of a yarn or nonwoven fabric which is coated with a superabsorbent polymer in an amount of up to 500 % SAP add-on. The yarn or nonwoven fabric is made of fibers having a non-round cross section. The fibers when in the form of a filament yarn have a specific volume of the filament yarn being greater than or equal to 1.50 cc/gm.

    Abstract translation: 吸收液体的复合纤维结构体是纱线或非织造织物的形式,其涂覆有高达500%的SAP附加剂的超吸收聚合物。 纱线或无纺布由具有非圆形横截面的纤维制成。 当以长丝纱形式的纤维具有大于或等于1.50cc / gm的长丝纱的比体积。

    SOLUBLE MAGNESIUM CATALYST FOR PREPARATION OF DIHYDROXY ESTERS
    239.
    发明申请
    SOLUBLE MAGNESIUM CATALYST FOR PREPARATION OF DIHYDROXY ESTERS 审中-公开
    用于制备二羟基酯的可溶性镁催化剂

    公开(公告)号:WO1997042153A1

    公开(公告)日:1997-11-13

    申请号:PCT/US1997007007

    申请日:1997-04-25

    CPC classification number: C07C67/44 Y10S502/512 C07C69/675

    Abstract: A catalyst and process for preparation of dihydroxy esters from specified hydroxy aldehydes is disclosed. In one embodiment, a catalyst liquid is provided which comprises from 10 percent to 60 percent magnesium salt of a specified alkanoic acid or acids, and from 90 percent to 40 percent of a particular alkanoic acid or acids, the molar ratio of alkanoic acid to magnesium salt being from 1.5 to 20.3. The catalyst solution or liquid contacts or is contacted with a specified hydroxy aldehyde under suitable reaction conditions to form the desired dihydroxy ester. In another embodiment, dihydroxy esters are derived from specified hydroxy aldehydes by first forming a magnesium catalyst containing liquid by reacting magnesium or magnesium oxide, under suitable conditions, with a suitable alkanoic acid or acids, the acid or acids being provided in excess in specified molar ratios. The magnesium salt-alkanoic acid liquid produced is then employed as a catalyst liquid to convert the respective hydroxy aldehyde under suitable reaction conditions to form the desired dihydroxy ester.

    Abstract translation: 公开了一种用于由特定羟基醛制备二羟基酯的催化剂和方法。 在一个实施方案中,提供了催化剂液体,其包含10%至60%的特定链烷酸或酸的镁盐和90%至40%的特定链烷酸或酸,链烷酸与镁的摩尔比 盐从1.5到20.3。 催化剂溶液或液体在合适的反应条件下与特定的羟基醛接触或接触以形成所需的二羟基酯。 在另一个实施方案中,二羟基酯衍生自特定的羟基醛,首先通过在合适的条件下使镁或氧化镁与合适的链烷酸或酸反应而形成含有液体的镁催化剂,酸或酸以规定的摩尔数过量提供 比。 然后将所生产的镁盐 - 链烷酸液体用作催化剂液体,以​​在合适的反应条件下转化相应的羟基醛以形成所需的二羟基酯。

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