聚丁二酸丁二醇酯在堆肥条件下的生物降解性能研究

根据ISO 14855的检测方法,研究了聚丁二酸丁二醇酯(PBS)在堆肥条件下的生物降解性能,结果 表明PBS具有良好的生物降解性,且其形态对其降解速率有显著的影响,降解速率:PBS粉末>PBS片>PBS 颗粒。对堆肥中的微生物进行分离鉴定,在所选堆肥中主要分离出四种菌株:杂色曲霉菌、青霉菌、芽包杆菌 和直杆高温多孢菌,它们对PBS的降解能力各不相同,其中最有效降解PBS的菌株是杂色曲霉菌。     

可生物降解交联聚合物的研究进展

交联聚合物具有稳定的三维网络结构,可以提高药物缓释载体的尺寸稳定性。本文综述了可生物降解交联聚合物的研究进展,主要介绍了可生物降解交联聚合物的制备方法,包括交联剂交联、辐照交联、光致交联以及过氧化物交联在制备可生物降解交联聚合物中的应用,详细介绍了交联剂的种类及结构对交联效果的影响、交联后聚合物性能的变化等。最后总结了可生物降解交联聚合物在组织工程支架、药物缓释材料、神经再生修复材料以及形状记忆材料等生物医用领域的应用。     

PBS基生物降解材料的研究进展

PBS(聚丁二酸丁二醇酯 )是一种具有良好生物降解性的聚酯塑料。本文简述了PBS的基本特性、降解机理和制备方法 ,对各种PBS基生物降解材料的特性进行了分析 ,介绍了PBS基生物降解材料的研究进展     

生物降解性聚酯

本文阐述了生物降解性聚酯的主要产品，生物降解性聚酯的降解机理及生物降解性聚合物的存在问题和研究方向．     

交联对CO_2共聚物为基的聚氨酯降解性能的影响

讨论了CO2 共聚物为基的聚氨酯 -聚碳酸亚乙酯聚氨酯 (PEC-PU)交联方式、交联程度对其生物降解性能的影响。实验结果显示 ,交联程度越大 ,降解程度有所降低 ,但一定交联程度的交联型PEC -PU仍然具有良好的生物降解性能。     

用木粉制备生物降解塑料的探讨

本文报道以木粉制备生物降解塑料的工艺，以及该塑料的机械性能和生物降解性能等情况。在摸索出的样品组成及加工工艺条件下制备的样品，其拉伸强度为5MP左右，冲击强度为2.0kJ／m~2左右。并具有一定的生物降解性能，在三个月内降解失重率为15％左右。     

纤维素纤维材料几种降解方法的研究

测试和比较了天然棉纤维织物和几种人造可再生纤维素纤维(竹原纤维、莫代尔纤维和天丝纤维)在实验室条件下和大环境堆肥条件下的生物降解性.生物降解行为的测试分别采用ASTM D5988-03、堆肥法和酶催化降解法,以比较几种织物在自然环境和微生物培养基条件下的降解速度;结合红外光谱通过分析降解前后结构的改变研究不同的降解方法对纤维素材料的降解程度.结果表明纤维素类纤维织物均表现出良好的生物降解性,并且人造可再生纤维素纤维的降解速度高于天然棉纤维.和传统的实验室条件下测量织物降解性的方法相比,堆肥中含有更多的微生物和酶活性组分,加速了纤维素材料的分解.     

生物降解PBS聚醋的改性研究进展

聚丁二酸丁二醇酯(PBS)是一种具有良好生物降解性的聚酯,本文简述了PBS的基础物性和力学性能,综述了各种改善PBS生物降解性、生物相容性、热学和力学性能的方法,重点介绍了通过共聚、共混等方法对PBS进行改性的研究进展.     

改性淀粉材料生物降解性分析体系的建立及应用

测定了热塑性淀粉(TPS)和热塑性双醛淀粉(TPDAS)在堆肥条件下的生物降解能力。根据ISO 14855建立了一套新的测试体系并且验证了这个体系测定高分子材料生物降解性能的可行性。对热塑性淀粉材料生物降解性的测试结果发现化学改性对于淀粉的降解速率和降解速度都有很大的影响。在可控堆肥条件下TPS比TPDAS降解的要快。TPDAS的降解速度和最终的生物降解百分率和双醛淀粉(DAS)的氧化度有密切的关系。文中讨论了存在这种关系的可能原因。有不同降解速率的TPS和TPDAS的降解过程呈现出三个阶段,即迟滞阶段。降解阶段和平稳阶段。     

苯乙烯-马来酸酐共聚物的生物降解性研究

合成了一系列苯乙烯．马来酸酐共聚物(SMA)。并对共聚物的结构进行了表征。用土埋法和CO2释放法研究了共聚物的生物降解性。探讨了分子量、组成、环境等因素对生物降解性的影响,发现共聚物的分子量降低。降解率增大;共聚物中马来酸酐含量提高。降解率增大;适宜的环境有利于生物降解。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.