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注射用阿奇霉素的成盐剂的研究 被引量:10
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作者 何琪莹 吕万良 张强 《中国抗生素杂志》 CAS CSCD 北大核心 2005年第4期204-207,共4页
目的选择适合的注射用阿奇霉素成盐剂。方法将阿奇霉素与8种酸制成溶液及冻干粉针剂,并通过对pH值、初步稳定性试验及在动物体内静脉滴注阿奇霉素与8种盐冻干制剂,比较其肝脏毒性,选择适当的成盐剂。结果谷氨酸、乳糖酸、酒石酸和天冬... 目的选择适合的注射用阿奇霉素成盐剂。方法将阿奇霉素与8种酸制成溶液及冻干粉针剂,并通过对pH值、初步稳定性试验及在动物体内静脉滴注阿奇霉素与8种盐冻干制剂,比较其肝脏毒性,选择适当的成盐剂。结果谷氨酸、乳糖酸、酒石酸和天冬氨酸与阿奇霉素的盐溶液较为稳定且pH值属于合适范围;动物试验显示各参比盐制剂病理结果均有不同程度的改变,表现较轻者有谷氨酸盐、柠檬酸盐、天冬氨酸盐、硫酸盐、盐酸盐,较重者有磷酸二氢盐、乳糖酸盐、酒石酸盐。结论谷氨酸、天冬氨酸均为合适的阿奇霉素成盐剂。 展开更多
关键词 阿奇霉素 成盐剂 稳定性 肝脏毒性
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苯甲异噁唑青霉素钠工艺革新——以醋酸钠代异辛酸钠作为成盐剂
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《医药工业》 CAS 1977年第Z2期47-47,共1页
我厂生产苯甲异噁唑青霉素钠(P12)原以异辛酸钠作为成盐剂。异辛酸钠系用异辛酸与氢氧化钠反应制得。异辛酸为短线原料,需要进口。去年3月我厂参照上海第三制药厂的经验,以甲醇、醋酸钠代异辛酸钠进行成盐反应,取得成功。在此基础上,... 我厂生产苯甲异噁唑青霉素钠(P12)原以异辛酸钠作为成盐剂。异辛酸钠系用异辛酸与氢氧化钠反应制得。异辛酸为短线原料,需要进口。去年3月我厂参照上海第三制药厂的经验,以甲醇、醋酸钠代异辛酸钠进行成盐反应,取得成功。在此基础上,我们又设法以水代甲醇,即用水、醋酸钠作为成盐剂,成盐反应也很顺利,收率较用甲醇、醋酸钠作成盐剂高2~3%,经进一步试验,现我们在生产中直接投入粉碎的结晶醋酸钠进行成盐反应,效果更好。 展开更多
关键词 异辛酸钠 成盐剂 醋酸钠 乙酸钠 工艺革新
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两种成盐方式合成的聚醚醚酮的表征及光谱研究 被引量:9
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作者 倪卓 郑玉斌 +1 位作者 吴忠文 汤心颐 《高分子材料科学与工程》 EI CAS CSCD 北大核心 1989年第3期64-68,共5页
聚醚醚酮(PEEK)是一种新型耐高温工程塑料。本文以K_2CO_3和K_2CO_3/Na_2CO_3混盐为成盐剂合成了PEEK,经过系统地表征和光谱的研究发现:前者存在少量支化结构,色泽不好,溶解性差;后者是全对位结构,色泽好,溶解性好。
关键词 聚醚醚酮 合成 成盐剂
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菁染料合成中碱性杂环中间体成盐方法的改进
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作者 王涛 黄德音 《影像技术》 CAS 1997年第2期33-34,共2页
本文寻找到一条有效的提高菁染料合成中碱性杂环中间体与成盐剂成盐反应效率的方法,该方法简便,易行反应转化率高,产品的性能好,更适合扩大生产。
关键词 碱性杂环中间体 菁染料 成盐 成盐剂 增感
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水性聚氨酯膜吸收CO_(2)矿化形成复合膜及其防腐蚀性能 被引量:4
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作者 董勇 姚皖生 +5 位作者 董晓宇 王兆飞 樊康鑫 张雪敏 李学良 丁运生 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2022年第5期9-16,共8页
以异佛尔酮二异氰酸酯(IPDI)、聚醚二元醇(PPG)和N,N-二甲基-N',N'-二(2-羟丙基)-1,3-丙二胺等为主要原料制备了聚氨酯预聚体,并利用乙酸、3-羧基-3-羟基戊二酸和2,2-二羟甲基丙酸(DMPA)为成盐剂与聚氨酯预聚体反应,产物经乳化... 以异佛尔酮二异氰酸酯(IPDI)、聚醚二元醇(PPG)和N,N-二甲基-N',N'-二(2-羟丙基)-1,3-丙二胺等为主要原料制备了聚氨酯预聚体,并利用乙酸、3-羧基-3-羟基戊二酸和2,2-二羟甲基丙酸(DMPA)为成盐剂与聚氨酯预聚体反应,产物经乳化得到3种阳离子水性聚氨酯胶乳(WPU1,WPU2和WPU3),并将其制膜后浸泡在模拟海水中。研究了3种水性聚氨酯膜吸收CO_(2)并矿化形成聚氨酯-碳酸钙(PU-CaCO_(3))复合膜的过程及防腐蚀性能。红外光谱分析结果表明,成功合成了3种阳离子水性聚氨酯。粒径分析表明,WPU1,WPU2和WPU3胶乳粒径大小分别为19.38 nm,93.08 nm和84.33 nm。X射线衍射、扫描电镜和电化学测试结果表明,WPU2和WPU3膜经模拟海水浸泡后表面出现CaCO_(3)矿化层,WPU3膜表面形成的矿化层较致密,且具有优良的防腐蚀性能,其腐蚀速率和腐蚀电流密度分别为1.70×10^(-3)mm/a和1.44×10^(-7)A/cm^(2)。 展开更多
关键词 水性聚氨酯 成盐剂 CO_(2) 矿化 复合膜 防腐蚀性能
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水性聚氨酯的合成及研究 被引量:2
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作者 张丕勇 《山西化工》 2012年第6期5-6,19,共3页
采用丙酮回流法合成水性聚氨酯。发现,在1,4-丁二醇(BDO)质量分数为5%~15%时,乳化状况较好;二羟甲基丙酸(DMPA)质量分数为5%~7%时,较易乳化;丙酮质量分数为50%时,可得到均匀稳定的浊液。同时,考察了成盐剂三乙胺和丁胺对乳液的影响,... 采用丙酮回流法合成水性聚氨酯。发现,在1,4-丁二醇(BDO)质量分数为5%~15%时,乳化状况较好;二羟甲基丙酸(DMPA)质量分数为5%~7%时,较易乳化;丙酮质量分数为50%时,可得到均匀稳定的浊液。同时,考察了成盐剂三乙胺和丁胺对乳液的影响,以三乙胺(TEA)为成盐剂时乳化效果较好。 展开更多
关键词 水性聚氨酯 成盐剂 乳浊液 合成
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头孢噻肟钠制备工艺的改进 被引量:4
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作者 孙津鸽 高得瀛 +2 位作者 刘红坤 李文杰 李志军 《山东化工》 CAS 2016年第4期12-13,共2页
为改进头孢噻肟钠制备工艺。在混合溶媒中,头孢噻肟酸与成盐剂反应制得头孢噻肟钠溶液,再滴加溶析剂析出头孢噻肟钠固体。制得头孢噻肟钠的含量稳定在96%以上,且目标产物经质谱和核磁共振确认结构。改进后的工艺优化了反应条件,提高了含... 为改进头孢噻肟钠制备工艺。在混合溶媒中,头孢噻肟酸与成盐剂反应制得头孢噻肟钠溶液,再滴加溶析剂析出头孢噻肟钠固体。制得头孢噻肟钠的含量稳定在96%以上,且目标产物经质谱和核磁共振确认结构。改进后的工艺优化了反应条件,提高了含量,降低了成本,更适合工业化生产。 展开更多
关键词 头孢噻肟酸 头孢噻肟钠 成盐剂 工艺改进
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头孢西丁钠结晶工艺研究 被引量:1
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作者 王道社 孙佃振 张涛 《化工管理》 2021年第18期117-118,共2页
文章重点针对西丁钠的结晶工艺进行研究,通过对成盐剂、结晶溶剂用量、结晶方式的研究以寻求产品质量的提升。旨在探索最佳工艺组合,得到质量优异的头孢西丁钠产品。
关键词 头孢西丁钠 成盐剂 结晶方式
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头孢噻肟钠结晶工艺的研究 被引量:4
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作者 赵洪娥 刘华 +1 位作者 蔡秋琴 乔俊华 《河北化工》 2013年第02X期9-10,16,共3页
通过筛选成盐剂和改变体系溶剂配比,优化了头孢噻肟钠结晶工艺条件,新工艺所得产品含量高,溶液颜色和产品澄清度均有明显提高,颗粒偏大且分布均匀,易干燥和产业化。
关键词 头孢噻肟钠 结晶 成盐剂
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Studies on Degradation Characteristic of LAS High-resistance Strain 被引量:3
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作者 陈宏伟 朱蕴兰 +4 位作者 苏贤岩 邵影 梁峙 曹泽红 林进 《Agricultural Science & Technology》 CAS 2007年第3期33-37,共5页
A IAS degradation strain with high resistance, which could take linear alkylbenzene sulphonate (LAS) as only carton origin for growth, was isolated from the drain canal of Hangao Detergent Plant of Xuzhou. The chara... A IAS degradation strain with high resistance, which could take linear alkylbenzene sulphonate (LAS) as only carton origin for growth, was isolated from the drain canal of Hangao Detergent Plant of Xuzhou. The characteristic of its degradation was researched and the results showed that the optimum conditions of this strain for degrading LAS were 30℃, pH 6.0, 150 ml solution in 500 ml triangle vase, 120 r/min, LAS concentration of 200 - 600 mg/L. The growth amount of the bacteria were up to 0. 443 ( OD400 ) and the degrading rate was up to 89.4%. The ability of the bacterium to degrade LAS could be as high as concentration of 1 200 mg/L. 展开更多
关键词 Linear alkylbenzene sulphonate (LAS) SURFACTANT Degradation strain ISOLATION BIODEGRADATION
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全氟正丙基乙烯基醚的合成研究
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作者 余锋 包俊 +1 位作者 王章明 赵景平 《有机氟工业》 CAS 2018年第2期11-13,共3页
全氟2-甲基-3-氧杂己酸盐在溶剂中加热脱羧制备全氟正丙基乙烯基醚,研究了溶剂、成盐剂、反应温度及溶剂与全氟2-甲基-3-氧杂己酸盐的质量比等因素对脱羧反应的影响。试验结果表明:以二乙二醇二甲醚作溶剂,碳酸钠作成盐剂,反应温度130~... 全氟2-甲基-3-氧杂己酸盐在溶剂中加热脱羧制备全氟正丙基乙烯基醚,研究了溶剂、成盐剂、反应温度及溶剂与全氟2-甲基-3-氧杂己酸盐的质量比等因素对脱羧反应的影响。试验结果表明:以二乙二醇二甲醚作溶剂,碳酸钠作成盐剂,反应温度130~140℃,溶剂与盐的质量比0.3~0.8为适宜的脱羧反应条件。 展开更多
关键词 全氟2-甲基-3-氧杂己酸盐 全氟正丙基乙烯基醚 成盐剂
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异辛酸钠市场动态
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作者 王荣耕 《精细化工原料及中间体》 2003年第9期37-37,共1页
异辛酸钠,白色固体,暴露在空气中极易吸潮。易溶于有机溶剂中。主要用于制药行业成盐剂。该产品生产工艺较为简单,广泛地应用于各种药物的成盐工艺。传统的成盐工艺是使用无机碱类,如碳酸钠,碳酸氢钠,碳酸钾等,由于这些产品不溶于有机... 异辛酸钠,白色固体,暴露在空气中极易吸潮。易溶于有机溶剂中。主要用于制药行业成盐剂。该产品生产工艺较为简单,广泛地应用于各种药物的成盐工艺。传统的成盐工艺是使用无机碱类,如碳酸钠,碳酸氢钠,碳酸钾等,由于这些产品不溶于有机溶剂。使产品的转化率受到影响,同时也容易进入产品而引入杂质。 展开更多
关键词 异辛酸钠 市场分析 药物 成盐工艺 成盐剂
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Kinetics of Methane Hydrate Formation in Pure Water and Inhibitor Containing Systems 被引量:6
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作者 裘俊红 郭天民 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2002年第3期316-322,共7页
Kinetic data of methane hydrate formation in the presence of purewater, brines with single salt and mixed salts, and aqueous solutionsof ethylene glycol (EG) and salt + EG were measured. A new kineticmodel of hydrate ... Kinetic data of methane hydrate formation in the presence of purewater, brines with single salt and mixed salts, and aqueous solutionsof ethylene glycol (EG) and salt + EG were measured. A new kineticmodel of hydrate formation for the methane + water systems wasdeveloped based on a four-step formation mechanism and reactionkinetics approach. The proposed kinetic model predicts the kineticbehavior of methane hydrate formation in pure water with goodaccuracy. The feasibility of extending the kinetic model to salt (s)and EG containing systems was explored. 展开更多
关键词 KINETICS hydrate formation INHIBITORS METHANE
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The carboxylates formed on oxides promoting the aromatization in syngas conversion over composite catalysts 被引量:1
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作者 Zhiyang Chen Youming Ni +3 位作者 Fuli Wen Ziqiao Zhou Wenliang Zhu Zhongmin Liu 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2021年第5期835-843,共9页
Syngas to aromatics(STA)over bifunctional catalysts has attracted much attention in recent years,but the mechanism underlying the formation of aromatics remains controversial.The critical reaction intermediates,carbox... Syngas to aromatics(STA)over bifunctional catalysts has attracted much attention in recent years,but the mechanism underlying the formation of aromatics remains controversial.The critical reaction intermediates,carboxylates,were first identified and then confirmed to essentially promote aromatization in the syngas conversion over a ZnCrAlO_(x)&H-ZSM-5 composite catalyst.This study provides evidence that the carboxylates can be formed during the reactions of formate species and olefins.In addition,it is shown that the carboxylates favor the formation of aromatics over H-ZSM-5 even in the presence of H2.A novel mechanism for the formation of aromatics via the generation and transformation of carboxylate intermediates is proposed,and the transformation of carboxylates to aromatics via methyl-2-cyclopenten-1-one(MCPO)intermediates is indeed likely.A better understanding of the formation mechanism of aromatics would help optimize the composite catalyst. 展开更多
关键词 CARBOXYLATES Syngas-to-aromatics Composite catalysts ZnCrAlO_(x) H-ZSM-5
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STUDY ON BEHAVIOUR OF CR FORMULATION OF THIOBENCANB IN A MODEL PADDY FIELD
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作者 孙锦荷 李兴明 +1 位作者 陈子元 张勤争 《Nuclear Science and Techniques》 SCIE CAS CSCD 1994年第1期7-14,共8页
The fate of CR formulation of 14C--thiobencarb (thio.) was studied at the high rate of application in a model paddy field. Thio. could be released from the alginate formulation (TAL-17189) into water. The concentratio... The fate of CR formulation of 14C--thiobencarb (thio.) was studied at the high rate of application in a model paddy field. Thio. could be released from the alginate formulation (TAL-17189) into water. The concentration of thio. in water increased with time, then declined. Thio. in water could be converted to more than 12 14C--degradation products which changed with time. An unknown degradation product (Mo) was always prevailing after application. Thio. in water could be adsorbed by soil particles. Most of the adsorbed thio. retained in upper layer. Thio. in soil could be also degraded tO more than 6 products. Thio. and its degradation products could conjugate with the compositions of soil to bound residues (BR). Thio. was 45.6 % of the toeal 14C--extractable residues (ER) in upper layer soil at harvest. 14C--thio. in water and soil could be uptaken by rice plants. Thio. in plants existed in ER and BR.Most of 14C--residues in straw, roots, brown rice and husk were in bound form, more than 92 % of the toeal 14C in them at harvest respectively. Thio. in plantS could be metabolized to more than 9 metsbolites which changed with time. 14C--thio. in straw,brown rice and husk accounted for 55\88, 6.06 and 11.18 % of the total 14C-- ER of them at harvest respectively. An unknown 14C--metebolite in brown rice was prevailing,accounted for 63.03 % of the total 14C- ER. 展开更多
关键词 Thiobencarb Controlled--release formulation Paddy field
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Adsorption of Metal Ions by Sorbents Composed of Marine Alga Saccharina bongardiana and Poriferous Aluminosilicates
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作者 Tatyana P. Belova Olga N. Selivanova 《Journal of Environmental Science and Engineering(A)》 2012年第4期514-521,共8页
The development of gold and cobalt-copper-nickel deposits in Kamchatka threatens the loss of biodiversity in spawning rivers and lakes and has negative effects on coastal ecosystems. To reduce pollution by mining wast... The development of gold and cobalt-copper-nickel deposits in Kamchatka threatens the loss of biodiversity in spawning rivers and lakes and has negative effects on coastal ecosystems. To reduce pollution by mining wastes, filters with dried marine alga Saccharina bongardiana in combination with zeolite and pumice are recommended. Combined Saccharina-based sorbents remove heavy metal ions more effectively, increasing adsorption capacity by five times compared to mineral (pumice) sorhents. As a result of desorption, a tenfold increase of the solution concentration is reached after the first sorption cycle. Valuable elements (Ni, Co, Cu etc.) can then be extracted from concentrates by any known method. It increases economic efficiency of the mining industry due to recycling of non-ferrous metals. Saccharina-based sorbents can be also utilized for purification of polluted natural waters. It may serve as environmental protection measure and provide for ecological safety of the unique natural environment of Kamchatka and its bioresources. 展开更多
关键词 Sorbents ZEOLITE PUMICE Saccharina bongardiana mining industry environmental protection.
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离子色谱法测定注射用氯唑西林钠中醋酸根离子含量 被引量:10
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作者 闻宏亮 赵敬丹 +3 位作者 秦峰 裘亚 刘浩 杨美成 《药物分析杂志》 CAS CSCD 北大核心 2016年第7期1268-1273,共6页
目的:建立离子色谱法测定注射用氯唑西林钠中醋酸根离子的含量。方法:采用TSKgel Super IC-AP阴离子柱(4.6 mm×150 mm,6μm),流动相为6.3 mmol·L^(-1)碳酸氢钠与1.1 mmol·L^(-1)碳酸钠的混合溶液,流速为0.8 m L·min... 目的:建立离子色谱法测定注射用氯唑西林钠中醋酸根离子的含量。方法:采用TSKgel Super IC-AP阴离子柱(4.6 mm×150 mm,6μm),流动相为6.3 mmol·L^(-1)碳酸氢钠与1.1 mmol·L^(-1)碳酸钠的混合溶液,流速为0.8 m L·min^(-1),柱温为35℃,进样体积为10μL,抑制型电导检测。结果:氟离子等常见无机离子、甲酸根离子以及强破坏(高温破坏、光照破坏、酸破坏、碱破坏及氧化破坏)降解产物均不干扰醋酸根离子的测定。醋酸根离子在0.990 0~99.00μg·m L^(-1)范围内峰面积与质量浓度线性关系良好(r=0.999 9);平均加样回收率(n=9)为99.5%,RSD为0.3%;方法最低定量限为0.002 5%。有6个厂家的22批样品采用醋酸钠作为成盐剂,相应样品中残留的醋酸根离子含量在0.07%~0.83%之间。结论:建立的离子色谱法可用于注射用氯唑西林钠中醋酸根离子的含量测定。 展开更多
关键词 醋酸根 注射用氯唑西林钠 半合成青霉素 2-乙基己酸 离子色谱法 成盐剂残留检测
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Oxygen-deficient bismuth tungstate and bismuth oxide composite photoanode with improved photostability 被引量:1
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作者 Hoi Ying Chung Weijian Chen +5 位作者 Xiaoming Wen Judy N. Hart Hao Wu Yuekun Lai Rose Amal Yun Hau Ng 《Science Bulletin》 SCIE EI CSCD 2018年第15期990-996,共7页
A homogeneous layer of Bi_2O_3-Bi_(14)WO_(24) composite(BWO/Bi_2O_3) thin film was fabricated using a combination of electrodeposition and thermal treatment. The evenly distributed Bi14 WO24 component within the Bi_2O... A homogeneous layer of Bi_2O_3-Bi_(14)WO_(24) composite(BWO/Bi_2O_3) thin film was fabricated using a combination of electrodeposition and thermal treatment. The evenly distributed Bi14 WO24 component within the Bi_2O_3 layer was found to be important in stabilising the photoelectrochemical performances of Bi_2O_3 photoanode by promoting the photoelectron transport. The unmodified Bi_2O_3 suffered from severe photocorrosion as proven by X-ray diffraction(XRD) and inductively coupled plasma(ICP) analyses while the composite thin film was active without noticeable activity decay for at least 3 h of illumination. This strategy might be applicable to other photocatalysts with stability issues. 展开更多
关键词 Bismuth oxide Bismuth tungstate PHOTOCORROSION
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Synthesis of a sulfur-graphene composite as an enhanced metal-free photocatalyst 被引量:6
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作者 Wenchao Peng Xiaoyan Li 《Nano Research》 SCIE EI CAS CSCD 2013年第4期286-292,共7页
A novel metal-free photocatalyst--sulfur/graphene (S/GR) composite--has been synthesized using a facile one-pot, two-step hydrothermal method with thiosulfate and graphene oxide (GO) as precursors. A green reducta... A novel metal-free photocatalyst--sulfur/graphene (S/GR) composite--has been synthesized using a facile one-pot, two-step hydrothermal method with thiosulfate and graphene oxide (GO) as precursors. A green reductant--L-ascorbic add--was used to transform GO to GR under mild conditions. The photocatalyst powders were characterized by Fourier transform infrared spectroscop, X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and energy dispersive spectroscopy. Experimental tests were conducted on the photocatalytic decomposition of methyl orange (MO) by different catalysts. Compared to pure oL-S, the as-prepared S/GR composite showed much enhanced photocatalytic activity for the degradation of MO under both UV and solar light. The presence of GR also greatly increased the hydrophilicity and adsorption capacity of the catalyst material. The results indicate that the incorporation of GR with a-S results in a synergistic effect for the S-based photocatalysts offering more effective environmental applications. 展开更多
关键词 metal-free catalyst a-sulfur GRAPHENE PHOTOCATALYSIS methyl orange organic degradation
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