共查询到20条相似文献,搜索用时 281 毫秒
1.
The calcium carbonate phases calcite, aragonite, vaterite, monohydrocalcite (calcium carbonate monohydrate), and ikaite (calcium carbonate hexahydrate) were studied by solid-state NMR spectroscopy ( (1)H and (13)C). Further model compounds were sodium hydrogencarbonate, potassium hydrogencarbonate, and calcium hydroxide. With the help of these data, the structure of synthetically prepared additive-free amorphous calcium carbonate (ACC) was analyzed. ACC contains molecular water (as H 2O), a small amount of mobile hydroxide, and no hydrogencarbonate. This supports the concept of ACC as a transient precursor in the formation of calcium carbonate biominerals. 相似文献
2.
Crystal growth of calcium carbonate in biological simulation was investigated via egg white protein with different volume fractions,during which calcium carbonate was synthesized by calcium chloride an... 相似文献
3.
Aspects on the interaction between sodium carboxymethylcellulose and calcium carbonate and the relationship to specific site adsorption 总被引:3,自引:0,他引:3
Backfolk K Lagerge S Rosenholm JB Eklund D 《Journal of colloid and interface science》2002,248(1):5-12
The mechanisms of adsorption and association for sodium carboxymethylcellulose (NaCMC) in calcium carbonate suspensions have been determined from isothermal calorimetry and adsorption measurements. The equilibrium adsorption isotherms were determined by two different methods of separation; a depletion method and a serum exchange method. The enthalpy of dilution for NaCMC was determined on supernatants obtained from the calcium carbonate suspensions in order to investigate the interaction between NaCMC and dissolved species from the mineral. For comparison, NaCMC was injected into CaCl(2) solutions in order to determine the role of calcium ions in the adsorption process. The initial part of the adsorption isotherm showed a quasi-infinite slope indicating a high affinity for the NaCMC to the calcium carbonate surface, which was significantly reduced when anionic sodium polyacrylate was preadsorbed onto the calcium carbonate implying competitive adsorption. An endothermic enthalpy change was observed between the NaCMC and the calcium carbonate surface, suggesting attachment of the carboxylic acid groups onto the hydrated calcium sites. A similar endothermic enthalpy was observed when NaCMC was injected into CaCl(2) solutions or supernatants obtained from the calcium carbonate suspensions, indicating a complexation of carboxylic acid groups and hydrated calcium ions. It was concluded that the mechanisms of interaction of NaCMC in calcium carbonate suspensions are primarily an association between NaCMC and Lewis acid sites on the calcium carbonate surface and the formation of NaCMC-Ca(2+) complexes in the bulk solution, both of which will be affected by the amount of anionic sodium polyacrylate present. 相似文献
4.
采用液相沉淀法,以硝酸铋[Bi(NO_3)_3]为添加剂来调控碳酸钙晶体的形状与大小,制备了海螺状碳酸钙粒子.通过扫描电子显微镜(SEM)、X射线衍射仪(XRD)、热重分析仪(TGA)、原子荧光光谱仪(AFS)等对产物的结构和性能进行了表征.结果表明,在60℃条件下,添加20 mL浓度为2 g/L的Bi(NO_3)_3溶液可得到海螺状球霰石型碳酸钙粒子,且其荧光性明显增强.在碳酸钙的成核过程中,Bi~(3+)的加入起到了显著的调控作用. 相似文献
5.
6.
7.
Jos Sepulcre‐Guilabert Teresa del Pilar Ferrandiz‐Gmez Jos Miguel Martín‐Martínez 《Macromolecular Symposia》2001,169(1):185-190
Natural ultramicronized calcium carbonate and mixtures of fumed silica‐natural ultramicronized calcium carbonate are proposed as fillers of solvent based polyurethane (PU) adhesives. PU adhesive containing only calcium carbonate shows similar rheological, thermal, mechanical, surface and adhesion properties than the PU adhesive without filler. Addition of 90 wt% fumed silica +10 wt% calcium carbonate mixture to PU adhesive produced a similar performance than the PU adhesive containing only famed silica. The increase in the amount of natural calcium carbonate in respect to fumed silica in the filler mixture produced detrimental effect on the rheological and mechanical properties of the PU adhesives (in respect to those provided by the PU adhesive only containing fumed silica), although the surface and adhesion properties were not noticeably modified. 相似文献
8.
It has been shown that an existing procedure to differentiate calcium oxide from the carbonate and silicate of calcium can be used in the presence of the phosphate, fluoride and sulphate of calcium, and of the carbonate and oxide of magnesium. It is based on the reaction in aqueous solution of calcium oxide with sucrose to form calcium saccharate, and subsequent titration with oxalic acid solution. The method has application for a direct chemical determination of calcium oxide in phosphate rock where calcination of accompanying carbonate is necessary in beneficiation processes. 相似文献
9.
The role of stabilizing agents in the interaction between styrene/butadiene latex and calcium carbonate particles has been studied using isothermal titration calorimetry (ITC) and an electrokinetic sonic amplitude (ESA) technique. It is demonstrated that the polyacrylate sodium salt (dispersing agent, referred to as NaPA) used as stabilizing agent for the calcium carbonate suspensions principally affects the interfacial properties of the calcite surface. An electrostatic barrier is created and this decreases the attractive interactions between the latex and the negatively charged mineral surface. The total enthalpy change observed when an emulsion of styrene/butadiene particles substantially free from surfactant was added to the dispersed calcium carbonate could be described via a relatively complex path. The process included (i) an exothermic response from the association of the latex particles (adsorption process) with the dispersed calcium carbonate surface and (ii) an endothermic bulk phase effect due to the adsorption on the latex particles of dissolved species originating from the calcium carbonate. Stabilization of the latex particles with sodium dodecyl benzene sulfonate (SDBS) or a non-ionic fatty alcohol ethoxylate surfactant did not significantly change the enthalpy of interaction. It was further demonstrated that SDBS had a very weak affinity for the dispersed calcium carbonate particles and that dissolution of species, such as calcium ions, from the calcium carbonate surface, allows further adsorption of SDBS onto the latex particles. 相似文献
10.
聚丙烯成核剂成核效应及热稳定性研究 总被引:6,自引:0,他引:6
为表征在聚合物材料热加工成型过程中成核剂的成核效果的热稳定性,设计了用反复升降温DSC实验,通过观察聚合物结晶温度和结晶热焓在反复升降温过程中的变化来考察成核剂的成核效率的稳定性.研究了碳酸钙、苯甲酸钠、对苯二甲酸和脂肪二元酸:庚二酸、辛二酸、壬二酸及其与碳酸钙组成的双组分成核剂对聚丙烯结晶成核效果的热稳定性.结果表明,高熔点物质碳酸钙、对苯二甲酸、苯甲酸钠的成核效果的热稳定性高,而脂肪二元酸的成核热稳定性低.庚二酸与碳酸钙组成的双组分成核剂的成核热稳定性高,但辛二酸、壬二酸与碳酸钙组成的双组分成核剂的成核热稳定性没有得到改善.这可能是由于庚二酸与碳酸钙之间存在某种相互作用,从而使成核效果得以稳定,而辛二酸、壬二酸与碳酸钙组成的双组分成核剂中,两个组分基本独立存在. 相似文献
11.
改性硝酸铵爆轰安全性研究 Ⅰ.CaCO3和MgSO4对硝酸铵爆轰安全性的影响 总被引:5,自引:0,他引:5
将碳酸钙和硫酸镁改性的硝酸铵按照工业炸药配方配制成铵油(ANFO)炸药,以8号雷管起爆,对硝酸铵的爆轰安全性进行了评价。采用恒温热分解和示差扫描量热法,研究了改性硝酸铵及铵油炸药的热分解行为。测定了改性硝酸铵的比表面积以解释爆轰结果。得出如下结论:硝酸铵含40%的碳酸钙,或25%碳酸钙和5%硫酸镁的混合物,所配制的铵油炸药不能被8号雷管起爆。碳酸钙同硝酸铵发生复分解反应放出NH3、H2O和CO2气体,反应程度与碳酸钙的含量、温度和时间成正比。虽然硝酸铵中加入碳酸钙后提高了ANFO炸药的热稳定性,但由于上述气体的逸出增加了改性硝酸铵的比表面积。因此,在硝酸铵中加入少量的碳酸钙不能达到爆轰安全性的要求。硫酸镁与硝酸铵形成复盐,可减缓硝酸铵和碳酸钙之间复分解反应的速度.有利于降低硝酸铵的起爆感度。 相似文献
12.
I. A. Pochitalkina P. A. Kekin A. N. Morozov D. F. Kondakov I. A. Petropavlovskii 《Russian Journal of Inorganic Chemistry》2016,61(11):1392-1396
The morphology of calcium carbonate prepared via homogeneous synthesis from carbonate–chloride solutions was studied. The precipitates were investigated by scanning electron microscopy (SEM) and Xray diffraction. The effects of the ratio between the chloride and carbonate components of a solution on the morphology, crystal structure, and particle size of precipitated calcium carbonate were illustrated. 相似文献
13.
Hideo Sawada Yasufumi Shikauchi Hiroshi Kakehi Yoshihiro Katoh Masashi Miura 《Colloid and polymer science》2007,285(5):499-506
Calcium chloride reacted with sodium carbonate in the presence of a variety of self-assembled molecular aggregates formed
by fluoroalkyl end-capped acrylic acid, 2-methacryloyloxyethane sulfonic acid, dimethylacrylamide, and acryloylmorpholine
oligomers in aqueous solutions to afford the corresponding fluorinated oligomers/calcium carbonate composites in excellent
to moderate isolated yields. These fluorinated calcium carbonate composites thus obtained were shown to have a good dispersibility
not only in water but also in traditional organic media including fluorinated solvents. Dynamic light scattering measurements
(DLS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that these fluorinated composites
are nanometer-size-controlled particles and well dispersed in these media. Cross-linked fluoroalkyl end-capped acrylic acid
co-oligomer containing poly(oxyethylene) units was also applied to the preparation of new cross-linked fluorinated calcium
carbonate nanocomposites under similar conditions. The obtained cross-linked fluorinated calcium carbonate nanocomposites
were found to have an extremely higher dispersibility in aqueous and organic media including fluorinated solvents, compared
to that of the corresponding fluoroalkyl end-capped oligomer nanocomposites. In particular, it was verified that these fluorinated
calcium carbonate nanocomposites are applicable to the dispersion above poly(methyl methacrylate) (PMMA) film surface. Interestingly,
field-emission SEM (FE-SEM) images of the cross-section of the modified PMMA films showed that calcium carbonate particles
dispersed into these PMMA films could be arranged regularly above the modified film surface. More interestingly, cross-linked
fluorinated oligomeric aggregates were able to provide suitable host moieties for the crystallization of calcium carbonate. 相似文献
14.
Dr. Julyan H. E. Cartwright Dr. Denis Gebauer Dr. C. Ignacio Sainz‐Díaz 《Angewandte Chemie (International ed. in English)》2012,51(48):11960-11970
Although the polymorphism of calcium carbonate is well known, and its polymorphs—calcite, aragonite, and vaterite—have been highly studied in the context of biomineralization, polyamorphism is a much more recently discovered phenomenon, and the existence of more than one amorphous phase of calcium carbonate in biominerals has only very recently been understood. Here we summarize what is known about polyamorphism in calcium carbonate as well as what is understood about the role of amorphous calcium carbonate in biominerals. We show that consideration of the amorphous forms of calcium carbonate within the physical notion of polyamorphism leads to new insights when it comes to the mechanisms by which polymorphic structures can evolve in the first place. This not only has implications for our understanding of biomineralization, but also of the means by which crystallization may be controlled in medical, pharmaceutical, and industrial contexts. 相似文献
15.
The synthesis and characterization of calcium carbonate microparticles by reaction of calcium chloride and ammonium bicarbonate in the presence of negatively charged phospholipid mixtures of negative and zwitterionic phospholipids has been reported. Negatively charged phospholipids influence the crystal morphology of calcium carbonate and induce the formation of thermodynamically less stable veterite polymorph as opposed to calcite polymorph. The phospholipids are entrapped in the calcium carbonate microparticles during the crystallization process, with a uniform distribution of phospholipids in the interior of the microparticles. This phenomenon was exploited to encapsulate a model hydrophobic fluorophore, the tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride complex, to simulate encapsulation of hydrophobic drug molecules. Thermogravimetric analysis reveals that, in these microparticles, the calcium carbonate and the phospholipid exhibit strong interactions. 相似文献
16.
17.
We developed a method to prepare hemispherical hollow silica microcapsules (HHSM) with different affinity surfaces using spherical vaterite calcium carbonate (SVCC) as a template. The preparation process composed of the adhesion of calcium carbonate onto the surface of methyl methacrylate (MMA) droplets followed by suspension polymerization, the partial etching of calcium carbonate on the polymethyl methacrylate (PMMA) mother particle, the formation of silicon dioxide powder by sol–gel reaction and their deposition onto the etched flat surface of calcium carbonate, the surface modification of deposited silicon dioxide with silane coupling agent, the removal of the mother particle with acetone, the formation of silicon dioxide powder by sol–gel reaction and deposition onto the exposed hemispherical surface of calcium carbonate, and the surface modification of deposited silicon dioxide with silane coupling agent. The synthesized microcapsules had a complete hemispherical structure and both hydrophilic and hydrophobic surfaces. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
18.
纳米产品(材料)是当今世界高科技产品之一.纳米碳酸钙作为粉体产品中的一种,以高纯、超细、改性和功能性为标志,广泛应用于橡胶、塑料、造纸、油墨、涂料、医药、化妆品等各行各业[1-2].主要用作填充材料,因粒度超细、分散性好,可以增加填充量,降低制品成本,改善制品性能,提高制品档次,拓宽制品使用范围.近年来,随着CaCO3的超细化、结构复杂化及表面改性技术的发展,极大地提高了它的应用价值.对不同形态的超细CaCO3制备技术的研究,已成为许多先进国家竞相开发的热点[3-5]. 相似文献
19.
CaCl2 encapsulated was placed in the hydrothermal reactor of an aqueous solution of Na2CO3 and dodecyl dimethyl benzyl ammonium bromide for synthesis of two samples of calcium carbonate by an improved hydrothermal method and one-pot method. Their crystal structure, morphology, chemical composition, and thermal stability of the synthesized samples of calcium carbonate were investigated by XRD, FTIR, SEM, EDS and TGDSC. The sterilization activity of the as-prepared samples was evaluated by killing of Sarcina lutea bacteria. The results indicated that the regular cube capsule-assisted calcium carbonate prepared by hydrothermal process was doped with dodecyl dimethyl benzyl ammonium bromide. Under the same condition, the spindle-shaped calcium carbonate synthesized the one-pot method was not doped with dodecyl dimethyl benzyl ammonium bromide. Among the samples of calcium carbonate, capsule-assisted calcium carbonate had shown better antibacterial effect for Sarcina lutea: in 48 h after its inhibition a zone diameter was 12.3 mm. 相似文献