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氧化铅 | 1317-36-8

中文名称
氧化铅
中文别名
一氧化铅;黄铅;三氧化二铅;黄色氧化铅;氧化铅(Ⅲ);黄丹;氧化铅(II);漳丹;粒状氧化铅;颗粒黄丹;C.I.颜料黄46;密陀僧
英文名称
lead(II) oxide
英文别名
lead monoxide;oxolead
氧化铅化学式
CAS
1317-36-8;1314-27-8;12059-89-1
化学式
OPb
mdl
——
分子量
223.199
InChiKey
YEXPOXQUZXUXJW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    886 °C(lit.)
  • 沸点:
    1470 °C
  • 密度:
    9.53
  • 溶解度:
    溶于浓碱、盐酸和氯化铵。不溶于稀碱和醇。
  • 暴露限值:
    a/nm
  • 物理描述:
    Litharge appears as odorless gray or yellow green or red-brown solid. Sinks in water. (USCG, 1999)
  • 颜色/状态:
    Exists in 2 forms: red to reddish-yellow, tetragonal crystals at ordinary temperature; yellow, orthorhombic crystals, stable above 489 °C
  • 蒸汽压力:
    1 Pa at 724 °C; 10 Pa at 816 °C; 100 Pa at 928 °C; 1kPa at 1065 °C; 10 kPa at 1241 °C; 100 kPa at 1471 °C
  • 稳定性/保质期:
    1. 如果遵照规格使用和储存,则不会分解,没有已知危险反应。避免氧化物或碱金属加热至300~450℃时变为四氧化三铅;继续升温又会变为一氧化铅。该物质不溶于水和乙醇,但能溶解于丙酮、硝酸、液碱及氯化铵中,并能与甘油发生硬化反应。有毒! 2. 操作过程中,请佩戴口罩,以阻滞95%~97%的铅粉尘。当蒸汽浓度较高时,应使用过滤式防毒面具或软管式防毒面具,并强制供给新鲜空气。工作时间内禁止进食、吸烟。工作后需洗浴并漱口、刷牙;使用1%醋酸溶液清洗手部或其他受污染部位以去除铅残留。若出现铅中毒症状,应及时脱离岗位,并根据严重程度调整工作岗位。β-PbO为黄色正交晶系晶体,两种形式均不溶于水和乙醇,微溶于稀硝酸。在常温下研磨时,α-PbO会转变为β-PbO;而β-PbO向α-PbO转变的温度范围是475~583℃。 3. 稳定 4. 禁配物:强酸、强碱 5. 聚合危害:不聚合
  • 分解:
    When heated to decomposition it emits toxic fumes of /lead/.

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    2
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

ADMET

代谢
铅通过吸入、口服和皮肤接触被吸收,然后主要分布到骨骼和红细胞中。在血液中,铅可能被发现与血清白蛋白或金属结合蛋白金属硫蛋白结合。有机铅通过细胞色素P-450酶代谢,而无机铅与δ-氨基酮戊酸脱水酶形成复合物。铅主要通过尿液和粪便排出。
Lead is absorbed following inhalation, oral, and dermal exposure. It is then distributed mainly to the bones and red blood cells. In the blood lead may be found bound to serum albumin or the metal-binding protein metallothionein. Organic lead is metabolized by cytochrome P-450 enzymes, whereas inorganic lead forms complexes with delta-aminolevulinic acid dehydratase. Lead is excreted mainly in the urine and faeces. (L136)
来源:Toxin and Toxin Target Database (T3DB)
代谢
铅通过吸入、口服和皮肤接触被吸收,然后主要分布到骨骼和红细胞中。在血液中,铅可能被发现与血清白蛋白或金属结合蛋白金属lothionein结合。有机铅通过细胞色素P-450酶代谢,而无机铅与δ-氨基酮酸脱氢酶形成复合物。铅主要通过尿液和粪便排出。
Lead is absorbed following inhalation, oral, and dermal exposure. It is then distributed mainly to the bones and red blood cells. In the blood lead may be found bound to serum albumin or the metal-binding protein metallothionein. Organic lead is metabolized by cytochrome P-450 enzymes, whereas inorganic lead forms complexes with delta-aminolevulinic acid dehydratase. Lead is excreted mainly in the urine and faeces. (L136)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 毒性总结
识别和使用:氧化铅存在两种形式:红色至红黄色的四方晶体和黄色的正交晶体。它用于制造蓄电池、陶瓷产品、油漆和橡胶。人类暴露和毒性:在一项中东研究中,报告了14名婴儿在使用含有91%氧化铅的传统药物Bint al Dahab后,早期婴儿期出现了急性铅脑病。将22名蓄电池厂工人的1至6岁儿童与22个邻近对照家庭的1至6岁儿童进行比较,以寻找铅吸收增加的证据。工人儿童的血铅和红细胞原卟啉值显著高于对照组儿童。对来自氧化铅工厂的44名男性工人的培养淋巴细胞进行了染色体分析,以及来自15名未暴露个体的对照组。暴露对象的血铅浓度范围为30至75微克/100毫升,对照组为15至35微克/10毫升。铅暴露时间从一个月到11年8个月不等。在职业暴露于铅的受试者中,发现了染色单体和染色体畸变的显著增加。这种发现的频率与铅暴露时间平行。动物研究:30只雄性和30只雌性仓鼠每周一次通过气管内注射1毫克氧化铅,单独或与1毫克苯并(a)芘一起注射10周。氧化铅单独诱导肺泡上皮化生(19)和腺瘤样增生(3)。与苯并(a)芘联合使用时,氧化铅在肺的外围区域引起腺瘤(9)和腺癌(1),以及肺泡上皮化生(23)和腺瘤样增生(5)。在雄性大鼠中,吸入氧化铅并不影响生育力,但精囊重量显著下降,这可能表明睾酮分泌模式的变化。在吸入铅的父系后代的雄性中,附睾精子数量减少,但这并不影响生育力。将家兔暴露于30微克/立方米的PbO,每天3小时,连续4天,然后在最后一次暴露后立即、24小时和72小时对其肺部进行灌洗。在灌洗液中测量的乳酸脱氢酶(肺细胞损伤的标志物)和溶酶体活性(溶酶体渗透性的标志物)在暴露后24小时和72小时显著增加。PbO产生中性粒细胞浸润。对巨噬细胞功能的影响也注意到了。生态毒性研究:氧化铅对蚯蚓(Eisenia fetida, Savigny)的行为、形态和病理学有显著影响。
IDENTIFICATION AND USE: Lead oxide exists in 2 forms: red to reddish-yellow, tetragonal crystals and yellow, orthorhombic crystals. It is used in manufacturing of storage batteries, ceramic products, paints, and rubber. HUMAN EXPOSURE AND TOXICITY: Acute lead encephalopathy in early infancy has been reported in a Middle Eastern study for 14 infants following the use of Bint al Dahab, a traditional medicine containing 91% lead monoxide. Twenty-seven one- to six-year-old children of 22 workers at a storage battery plant at high risk of exposure to lead oxide were compared with 32 one- to six-year-old children in 22 neighborhood control families for evidence of increased lead absorption. Workers' children had significantly higher blood lead and erythrocyte protoporphyrin values than control children. Chromosomes were analyzed in cultured lymphocytes of 44 male workers from a lead oxide factory, and from a control group of 15 nonexposed individuals. Lead concentration in blood ranged from 30 to 75 ug/100 mL in exposed subjects and from 15 to 35 ug/10 mL in controls. Length of exposure to lead ranged from one month to 11 years eight months. In subjects occupationally exposed to lead, a significant increase in chromatid and chromosome aberrations was found. The frequency of such findings parallels exposure time to lead. ANIMAL STUDIES: 30 male and 30 female hamsters were intratracheally injected with 1 mg lead oxide, alone or with 1 mg benzo(a)pyrene once a wk for 10 wk. Lead oxide alone induced alveolar metaplasia (19) and adenomatous proliferation (3) in the lungs. In combination with benzo(a) pyrene, lead oxide caused adenoma (9) and adenocarcinomas (1) in the peripheral area of the lungs, as well as alveolar metaplasia (23) and adenomatous proliferation (5). In male rats inhalation of lead oxide did not affect fertility, but seminal vesicle weight dropped significantly, which might suggest an alteration in the pattern of testosterone secretion. In the male progeny of sires that inhaled lead, the number of epididymal spermatozoa decreased but this did not interfere with fertility. Rabbits exposed to PbO at 30 ug/cu m for 4 days (3 hr/day) were sacrificed and their lungs lavaged immediately, 24 hr, and 72 hr after the final exposure. Lactate dehydrogenase (a marker of lung cell damage) and lysozyme activity (a marker of lysosome permeability), measured in the lavage fluid, were significantly increased 24 and 72 hr after exposure. PbO produced neutrophil infiltration. Effects on macrophage functions were also noted. ECOTOXICITY STUDIES: Lead oxide has a significant effect on behavior, morphology, and histopathology of earthworms (Eisenia fetida, Savigny).
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 毒性总结
铅模仿其他生物学上重要的金属,如锌、钙和铁,作为许多相应酶促反应的辅因子与之竞争。例如,铅已被证明能竞争性地抑制钙与钙调蛋白的结合,干扰神经递质的释放。它在对NMDA受体和蛋白激酶C上也表现出类似的竞争性抑制作用,这损害了大脑微血管的形成和功能,并改变了血脑屏障。铅还通过影响多巴胺合成的调节和阻止乙酰胆碱的诱发释放来影响神经系统。然而,其主要作用机制是通过抑制delta-aminolevulinic酸脱氢酶,该酶在血红素生物合成中至关重要,而血红素是血红蛋白必需的辅因子。(T4, A20, A22, L136)
Lead mimics other biologically important metals, such as zinc, calcium, and iron, competing as cofactors for many of their respective enzymatic reactions. For example, lead has been shown to competitively inhibit calcium's binding of calmodulin, interferring with neurotransmitter release. It exhibits similar competitive inhibition at the NMDA receptor and protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. Lead also affects the nervous system by impairing regulation of dopamine synthesis and blocking evoked release of acetylcholine. However, it's main mechanism of action occurs by inhibiting delta-aminolevulinic acid dehydratase, an enzyme vital in the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (T4, A20, A22, L136)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 毒性总结
铅模仿其他生物学上重要的金属,如锌、钙和铁,作为许多相应酶促反应的辅因子与之竞争。例如,铅已被证明能竞争性地抑制钙与钙调蛋白的结合,干扰神经递质的释放。它在对NMDA受体和蛋白激酶C的竞争中表现出类似的抑制,这损害了脑微血管的形成和功能,同时也改变了血脑屏障。铅还通过损害多巴胺合成的调节和阻止乙酰胆碱的诱发释放来影响神经系统。然而,其主要作用机制是通过抑制δ-氨基酮酸脱氢酶,这是一种在血红素生物合成中至关重要的酶,而血红素是血红蛋白必不可少的辅因子。(T4, A20, A22, L136)
Lead mimics other biologically important metals, such as zinc, calcium, and iron, competing as cofactors for many of their respective enzymatic reactions. For example, lead has been shown to competitively inhibit calcium's binding of calmodulin, interferring with neurotransmitter release. It exhibits similar competitive inhibition at the NMDA receptor and protein kinase C, which impairs brain microvascular formation and function, as well as alters the blood-brain barrier. Lead also affects the nervous system by impairing regulation of dopamine synthesis and blocking evoked release of acetylcholine. However, it's main mechanism of action occurs by inhibiting delta-aminolevulinic acid dehydratase, an enzyme vital in the biosynthesis of heme, which is a necesssary cofactor of hemoglobin. (T4, A20, A22, L136)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 致癌性证据
无机铅化合物对人类具有有限的致癌性证据。...无机铅化合物对实验动物具有充分的致癌性证据。醋酸铅、亚醋酸铅、铬酸铅和磷酸铅对实验动物具有充分的致癌性证据。对于氧化铅和砷酸铅,实验动物的致癌性证据不足。...对于铅粉,实验动物的致癌性证据不足。总体评估无机铅化合物可能对人类具有致癌性(2A组)。/无机铅化合物/
There is limited evidence in humans for the carcinogenicity of inorganic lead compounds. ... There is sufficient evidence in experimental animals for the carcinogenicity of inorganic lead compounds. There is sufficient evidence in experimental animals for the carcinogenicity of lead acetate, lead subacetate, lead chromate, and lead phosphate. There is inadequate evidence in experimental animals for the carcinogenicity of lead oxide and lead arsenate. ... There is inadequate evidence in experimental animals for the carcinogenicity of lead powder. Overall evaluation Inorganic lead compounds are probably carcinogenic to humans (Group 2A). /Inorganic lead compounds/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 致癌性证据
分类:B2;可能的人类致癌物。分类依据:足够的动物证据。十项大鼠生物测试和一项小鼠测试显示,通过饮食和皮下接触多种可溶性铅盐,肾肿瘤统计学上显著增加。动物测试在多个实验室、多种大鼠品系中提供了可重复的结果,并且有一些多肿瘤位点的证据。短期研究表明铅影响基因表达。人类致癌性数据不足。人类致癌性数据:不足。动物致癌性数据:足够。/基于以前分类系统的铅和化合物(无机)/
CLASSIFICATION: B2; probable human carcinogen. BASIS FOR CLASSIFICATION: Sufficient animal evidence. Ten rat bioassays and one mouse assay have shown statisticlly significant increases in renal tumors with dietary and subcutaneous exposure to several soluble lead salts. Animal assays provide reproducible results in several laboratories, in multiple rat strains with some evidence of multiple tumor sites. Short term studies show that lead affects gene expression. Human evidence is inadequate. HUMAN CARCINOGENICITY DATA: Inadequate. ANIMAL CARCINOGENICITY DATA: Sufficient. /Lead and Compounds (inorganic), Based on former classification system/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
这项研究旨在调查铅氧化物(PbO)粉末的经皮渗透性,以及使用两种不同洗涤剂进行快速皮肤去污的效果。使用Franz细胞在24小时内研究PbO通过人皮肤的体外渗透情况。在接触开始后30分钟,进行了有无去污的测试,去污分别使用象牙液体肥皂或一种新的实验性清洁剂。我们确认PbO可以透过皮肤,中位渗透量为2.9 ng/cm(第25-75百分位数为0.35-6)。使用象牙液体肥皂的清洁程序显著增加了皮肤渗透,中位值为23.6 ng/cm(第25-75百分位数为12-47.1;Mann-Whitney U检验,P = 0.0002),而新的实验性清洁剂仅略微增加了渗透(7.1 ng/cm)。我们的结果表明,有必要防止皮肤污染的发生,因为即使是短暂的接触,如果随后迅速清洗,也会增加皮肤含量和渗透。这项研究表明PbO粉末可以透过皮肤,并且在接触30分钟后进行的皮肤去污并没有减少24小时内发生的皮肤吸收,强调了在使用有毒物质时防止皮肤污染的必要性。
The aim of this study was to investigate the percutaneous penetration of lead oxide (PbO) powder and the effect of rapid skin decontamination with two different detergents. Franz cells were used to study in vitro PbO skin penetration through human skin during a 24-hour period. The tests were performed without or with decontamination using either Ivory Liquid soap or a new experimental cleanser 30 minutes after the start of exposure. We confirm that PbO can pass through the skin with a median penetration of 2.9 ng/cm (25-75th percentiles 0.35-6). The cleaning procedure using Ivory Liquid soap significantly increased skin penetration with a median value of 23.6 ng/cm (25-75th percentiles 12-47.1; Mann-Whitney U test, P = 0.0002), whereas the new experimental cleanser only marginally increased penetration (7.1 ng/cm). Our results indicate that it is necessary to prevent skin contamination from occurring because a short contact can increase skin content and penetration even if quickly followed by washing. This study demonstrated that PbO powder can pass through the skin and that skin decontamination done after 30 minutes of exposure did not decrease skin absorption occurring over 24 hours and stresses the need to prevent skin contamination when using toxic substances.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
14名男性志愿者每天暴露于氧化铅气溶胶23小时,平均浓度为10.9微克/立方米,持续最多17周。空气对铅血水平的贡献大约是每100毫升血液中1.4微克铅,对应于每立方米1微克铅。
14 male volunteers were exposed to a lead oxide aerosol for 23 hr per day at an average concentration of 10.9 ug/cu m for up to 17 weeks. ... The air contribution to the lead blood levels was approx 1.4 ug of lead per 100 mL blood per 1 ug of lead per cu m.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
从大鼠喂养研究中获得的数据表明,铅被摄入到大鼠股骨中的程度高度依赖于所给予铅的化学形态。铅醋酸盐的生物利用度最高,氧化铅次之,硫化铅和阿拉斯加混合矿石浓缩物的生物利用度最低。这种摄取与所研究的剂量范围内呈线性相关。
Data obtained from a feeding study in rats /showed that/ lead uptake into rat femurs was highly dependent on the chemical form of lead administered. Bioavailability was highest for lead acetate, intermediate for lead oxide, and lowest for lead sulfide and Alaskan mixed ore concentrate. This uptake was linearly related to dose over the range studied.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
这项研究的目的是确定包括硫酸铅、氧化铅、铅粉和硬脂酸铅在内的铅化合物的经皮吸收情况。通过皮肤剥离法测量了10名铅酸电池工人的皮肤表面的铅含量,并通过四种铅化合物(硫酸铅、氧化铅、铅粉和硬脂酸铅)的表皮应用测量了大鼠尿铅含量。在铅工的背部手和背部的第9和第10次皮肤剥离中发现了大量的铅。背手上的铅含量与血液中的铅含量显著相关(n = 10, r^2 = 0.66, p < 0.05,线性回归)。在大鼠中,铅化合物应用12天后,尿液中的总铅量显著增加,硬脂酸铅为146.0 + 或 - 6.4 ng(标准差),硫酸铅为123.1 + 或 - 7.2 ng,氧化铅为115.9 + 或 - 5.3 ng,铅粉为47.8 + 或 - 6.9 ng,对照组为10.3 ng,这表明有显著的皮肤吸收。结论是,大量的无机铅化合物可以通过皮肤吸收,因此在铅作业或任何污染环境中应仔细考虑皮肤保护。
The objective of this study was to determine percutaneous absorption of lead compounds, including lead sulfate, lead oxide, lead powder, and lead stearate. The lead content on the skin surface of 10 lead-battery workers was measured by the method of skin stripping, and urinary lead content of rats was measured with epicutaneous application of four lead compounds: lead sulfate, lead oxide, lead powder, and lead stearate. There were significant amounts of lead on the 9th and 10th skin strippings of the dorsal hand and the back of lead workers. The amount of lead on the dorsal hand was significantly correlated with the amount in the blood (n = 10, r 2 = 0.66, p < 0.05, linear regression). In rats, after lead compounds were applied for 12 days, total lead amount in urine significantly increased to 146.0 + or - 6.4 ng (SD) for lead stearate, 123.1 + or - 7.2 ng for lead sulfate, 115.9 + or - 5.3 ng for lead oxide, 47.8 + or - 6.9 ng for lead powder, and 10.3 ng for the control, which indicated significant skin absorption. It was concluded that significant amounts of inorganic lead compounds can be absorbed through the skin, and skin protection in lead-working or any contaminated environment should be carefully considered.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • TSCA:
    Yes
  • 危险等级:
    6.1(b)
  • 危险品标志:
    T,N
  • 安全说明:
    S45,S53,S60,S61
  • 危险类别码:
    R61,R33,R20/22,R50/53,R62
  • WGK Germany:
    3
  • 海关编码:
    2824 10 00
  • 危险品运输编号:
    UN 1479/2291
  • 危险类别:
    6.1(b)
  • 包装等级:
    III

SDS

SDS:90001fdcbf65be1ee4ff52fe5abad3ef
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第一部分:化学品名称

制备方法与用途

一氧化铅,一般称为黄丹,可用于颜料、光学玻璃、陶瓷、橡胶、油漆催干剂、石油业、铅盐和粘合剂等行业。

毒性 参见一氧化铅。早期中毒症状包括齿龈边缘出现铅线(明显中毒时可能没有铅线)、皮肤呈土灰色。初期可能出现神经衰弱综合征,如果影响小脑,则可能导致铅中毒性抑郁症或躁狂症,并引发铅毒性麻痹和敏感性多发性神经炎。还会影响低色素贫血、代谢及内分泌障碍、消化系统等。

  • 神经系统:抑制某些酶的活性,导致消化不良,腹部剧烈疼痛,肝脏受损。
  • 内分泌系统:可能引起高血压和胆固醇增高。

如果出现腹痛,可进行皮下注射阿托品等药物,并采取腹部保暖、灌肠或洗热水浴等措施。空气中最大容许浓度为0.01 mg/m³。

操作时应戴上口罩以减少95%~97%的铅粉尘吸入;当蒸汽浓度过高时,则需使用过滤式防毒面具或软管式防毒面具,并确保新鲜空气供应。工作期间禁止进食和吸烟,结束后要洗淋浴、漱口和刷牙。手部或其他部位如有污染,应用1%醋酸溶液清洗。严重中毒者应暂时离开工作岗位。

化学性质 黄丹为黄色四方晶系粉末,不溶于水及乙醇,但可溶于丙酮、硝酸、液碱或氯化铵中。

用途 广泛用于冶炼金属铅、制铅玻璃和铅化合物、催化剂以及油漆催干剂;作为分析试剂、硅酸盐的助熔剂,也适用于氨基酸沉淀;在电子管、显像管、光学玻璃及防辐射橡胶制品制造中有应用价值;是聚氯乙烯塑料稳定剂的重要原料;还用于蓄电池极板制造与石油精制等。

生产方法 采用金属铅氧化法:将铅加热熔融制成铅粒,然后在170~210℃下进行磨粉处理,在600℃以上高温焙烧以实现氧化反应。 [ 2Pb + O_2 \rightarrow 2PbO ]

类别 有毒物品

毒性分级 高毒

急性毒性 腹腔注射-大鼠LDL0: 430 毫克/公斤;腹腔注射-小鼠LD50: 217 毫克/公斤

刺激数据 皮肤接触-兔子,100毫克/24小时为轻度刺激。

可燃性危险特性 不可燃物质;受热时产生有毒含铅化物烟雾。

储运特性 储存于通风干燥的库房中,并与食品添加剂分开存放。

灭火剂 使用水、泡沫、砂土或二氧化碳进行灭火。

职业标准 TLV-TWA 0.15 毫克/立方米;STEL 0.04 毫克/立方米。

上下游信息

反应信息

  • 作为反应物:
    描述:
    氧化铅 以950%的产率得到
    参考文献:
    名称:
    PAVLOV, D.;MONAKHOV, B.;MAJA, M.;PENAZZI, N., J. ELECTROCHEM. SOC., 136,(1989) N, C. 27-33
    摘要:
    DOI:
  • 作为产物:
    描述:
    碳酸铅(II) 以99%的产率得到
    参考文献:
    名称:
    NYITRAI, ZOLTAN;FILIP, LIVIU;ILLES, STEFAN;PASOI, NICOLAE;MAZUR, STEFAN
    摘要:
    DOI:
  • 作为试剂:
    描述:
    一氧化碳苯酚氧化铅bis(acetylacetonato)palladium(II)四甲基氢氧化铵四丁基硝酸铵manganese(III) acetylacetonate 氧气 作用下, 100.0 ℃ 、11.0 MPa 条件下, 反应 3.0h, 生成 碳酸二苯酯
    参考文献:
    名称:
    Method and catalyst composition for producing aromatic carbonates
    摘要:
    本发明揭示了一种从芳香族羟基化合物经济生产芳香族碳酸酯的方法和催化剂组合物。本发明提供了一种羰基化芳香族羟基化合物的方法,包括将至少一种芳香族羟基化合物与氧气和一氧化碳接触,在无卤素羰基化催化剂组合物的存在下,所述无卤素羰基化催化剂组合物包括至少一种第8、9或10族金属源的有效量,至少一种第14族金属源的有效量的第一无机共催化剂,一种盐类共催化剂的有效量,以及可选的来自由第4族金属源、第7族金属源、第11族金属源和镧系元素源组成的羰基化催化剂组合物的第二无机共催化剂的有效量,以及可选的碱的有效量。本方法和催化剂组合物的一个重要优点是,在反应混合物中不含或不需要卤素以获得催化活性。
    公开号:
    US06700008B2
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文献信息

  • Characterization of the chemiluminescence observed during the reaction between lead vapor and 3ΣO2
    作者:E.A. Dorko、J.W. Glessner、C.M. Ritchey、S.R. Snyder
    DOI:10.1016/0009-2614(84)85392-0
    日期:1984.8
    The chemiluminescence observed during the reaction between lead vapor and ground state oxygen (13ΣO 2) was analyzed. The spectral bands could be assigned to transitions from the a, A, B and C electronic states to the ground state. Evidence is presented to indicate that the reactive lead vapor is generated thermally rather than electrically.
    铅蒸气和基态氧(之间的反应过程中观察到化学发光1 3 σ0 2)进行了分析。可以将光谱带分配给从a,A,B和C电子态到基态的跃迁。证据表明反应性铅蒸气是热产生的,而不是电产生的。
  • Analysis of the chemiluminescence from electronically excited lead oxide generated in a flow tube reactor
    作者:E.A. Dorko、J.W. Glessner、C.M. Ritchey、L.L. Rutger、J.J. Pow、L.D. Brasure、J.P. Duray、S.R. Snyder
    DOI:10.1016/0301-0104(86)80007-6
    日期:1986.3
    The chemiluminescence from electronically excited lead oxide formed during the reaction between lead vapor and either 3Σ O2 or O2 has been studied. The reactions were accomplished in a flow tube reactor. A microwave discharge was used to generate O2. The vibronic spectrum was analyzed and the band head assignments were used in a linear least-squares calculation to obtain the vibronic molecular
    从铅蒸气和任一之间的反应过程中形成的电子激发氧化铅化学发光3 ΣÒ 2或1 ΔÒ 2进行了研究。反应在流管反应器中完成。微波放电用于生成1 ΔÒ 2。分析了电子频谱,并将带头分配用于线性最小二乘计算,以获得铅的X,a,b,A,B,C,C',D和E的电子分子常数氧化物。基于这些和其他分子常数,计算了到基态跃迁以及Aa和Da跃迁的Franck-Condon因子。提出的证据支持在流管反应器中遇到的实验条件下导致化学发光的机理的动力学分析。前面介绍的机制已由当前数据验证。
  • Process for the production of basic soaps of divalent metals in powder
    申请人:Neynaber Chemie GmbH
    公开号:US04927548A1
    公开(公告)日:1990-05-22
    Powdered basic metal soaps having a composition corresponding to the formula (MO).sub.n.M(RCOO).sub.2, where MO represents CaO, ZnO, MgO, BaO, PbO, or a mixed oxide PbO/CaO, CaO/ZnO, BaO/CdO, or BaO/ZnO, M is one of the metals mentioned above, RCOO represents an anion of a fatty acid containing 8 to 34 carbon atoms, and n has a value of 0.2 to 2, may be obtained by reaction of powdered fatty acids with powdered metal oxides in the presence of small amounts of water, alcohol, and/or an acid at temperatures between ambient temperature and 100.degree. C. and under a pressure not greater than ambient. Preferably, there is continuous removal of water formed during the reaction, and the reaction mixture is present as free flowing particles throughout the reaction.
    具有符合公式(MO).sub.n.M(RCOO).sub.2的组成的粉状基本金属肥皂,其中MO代表CaO,ZnO,MgO,BaO,PbO或混合氧化物PbO / CaO,CaO / ZnO,BaO / CdO或BaO / ZnO,M是上述金属之一,RCOO代表含有8至34个碳原子的脂肪酸根离子,n的值为0.2至2,可以通过在微量水,酒精和/或酸的存在下,在常温和100℃之间的温度下,与金属氧化物粉末反应而得到。最好在反应过程中持续去除形成的水,并且反应混合物在整个反应过程中均为自由流动颗粒。
  • Method for the preparation of IV-VI semiconductor nanoparticles
    申请人:Cho Kyung-Sang
    公开号:US20060110313A1
    公开(公告)日:2006-05-25
    A high temperature (on the order of about 90° C. or above) non-aqueous synthetic procedure for the preparation of substantially monodisperse IV-VI semiconductor nanoparticles (quantum dots) is provided. The procedure includes first introducing a first precursor selected from the group consisting of a molecular precursor of a Group IV element and a molecular precursor of a Group VI element into a reaction vessel that comprises at least an organic solvent to form a mixture. Next, the mixture is heated to a temperature of about 90° C. or above and thereafter a second precursor which is different from the first precursor and is selected from the group consisting of a molecular precursor of a Group IV element and a molecular precursor of a Group VI element is added into the heated mixture. The reaction mixture is then mixed to initiate nucleation of IV-VI nanocrystals and the temperature of the reaction mixture is controlled to provide substantially monodispersed IV-VI nanoparticles having a diameter of about 20 nm or less.
    提供了一种高温(大约90°C或以上)的非水合成方法,用于制备基本单分散的IV-VI半导体纳米颗粒(量子点)。该方法首先将选自Group IV元素的分子前体或Group VI元素的分子前体之一的第一前体引入至至少包含有机溶剂的反应容器中形成混合物。接下来,将混合物加热至大约90°C或以上,然后向加热的混合物中加入与第一前体不同的第二前体,所述第二前体选自Group IV元素的分子前体或Group VI元素的分子前体之一。然后混合反应物以启动IV-VI纳米晶的成核,并控制反应物的温度,以提供直径约为20nm或更小的基本单分散的IV-VI纳米颗粒。
  • [1-Oxo-2-thienyl-2-substituted-5-indanyloxy (or thio)]alkanoic acids and
    申请人:Merck & Co., Inc.
    公开号:US04177285A1
    公开(公告)日:1979-12-04
    [1-Oxo-2-aryl or thienyl-2-substituted-5-indanyloxy (or thio)]alkaoic acid, derivatives thereof, their salts, esters and amides are disclosed. The products display a dual pharmaceutical utility in that they exhibit diuretic, saluretic and uricosuric activity. Also disclosed are processes for the preparation of such [1-oxo-2-aryl or thienyl-2-substituted-5-indanyloxy (or thio)]alkanoic acids, pharmaceutical compositions comprising therapeutically effective amounts of such compounds and methods of treatment comprising administering such compounds and compositions.
    本发明揭示了[1-氧代-2-芳基或噻吩基-2-取代-5-吲哚氧(或硫)基]脂肪酸及其衍生物、盐、酯和酰胺。该产品具有双重药物效用,表现出利尿、排盐和利尿酸活性。还揭示了制备这种[1-氧代-2-芳基或噻吩基-2-取代-5-吲哚氧(或硫)基]脂肪酸的方法、包含治疗有效量的这种化合物的药物组合物以及包括给予这种化合物和组合物的治疗方法。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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